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Bayer AG

Quarterly Report May 3, 2018

48_10-q_2018-05-03_c590c3c7-3686-43f8-9886-e97a24bc750f.pdf

Quarterly Report

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First Quarter of 2018

Bayer Group Key Data

Full Year
€ million Q1 2017 Q1 2018 Change % 2017
Sales 9,680 9,138 – 5.6 35,015
Change (adjusted for currency and portfolio effects) 1 + 2.0 + 1.5%
Change in sales 1
Volume + 4.5% + 3.2% + 2.3%
Price + 0.4% – 1.2% – 0.8%
Currency + 2.5% – 7.5% – 1.4%
Portfolio + 0.1% – 0.1% + 0.1%
EBITDA1 2,999 2,818 – 6.0 8,563
Special items 1 (55) (78) (725)
EBITDA before special items 1 3,054 2,896 – 5.2 9,288
EBITDA margin before special items 1 31.5% 31.7% 26.5%
EBIT1 2,427 2,310 – 4.8 5,903
Special items 1 (102) (78) (1,227)
EBIT before special items 1 2,529 2,388 – 5.6 7,130
Financial result (296) 130 (1,326)
Net income (from continuing and discontinued operations) 2,083 1,954 – 6.2 7,336
Earnings per share1 from continuing and discontinued operations (€) 2.39 2.24 – 6.3 8.41
Core earnings per share1 from continuing operations (€) 2.31 2.28 – 1.3 6.74
Net cash provided by operating activities
(from continuing and discontinued operations)
841 658 – 21.8 8,134
Cash outflows for capital expenditures 415 349 – 15.9 2,418
Research and development expenses (1,094) (1,040) – 4.9 4,504
Depreciation, amortization and impairments 572 508 – 11.2 2,660
Number of employees at end of period2 99,860 100,110 + 0.3 99,820
Personnel expenses (including pension expenses) 2,636 2,438 – 7.5 9,528

2017 figures restated

For definition see Annual Report 2017, A 2.4 "Alternative Performance Measures Used by the Bayer Group."

2 Employees calculated as full-time equivalents (FTEs)

Contents

Bayer Group Key Data _______________ 2
Interim Group Management Report as of March 31, 2018 ______ 5
1. Overview of Sales, Earnings and Financial Position ________ 5
1.1 Earnings Performance of the Bayer Group __________ 5
1.2 Business Development by Segment __________ 8
1.3 Asset and Financial Position of the Bayer Group __________ 16
2. Research, Development, Innovation _________ 18
3. Report on Future Perspectives and on Opportunities and Risks ________ 21
3.1 Future Perspectives ___________ 21
3.2 Opportunities and Risks ______________ 22
Condensed Consolidated Interim Financial Statements as of March 31, 2018 ____ 23
Bayer Group Consolidated Income Statements _________ 23
Bayer Group Consolidated Statements of Comprehensive Income __________ 24
Bayer Group Consolidated Statements of Financial Position _________ 25
Bayer Group Consolidated Statements of Cash Flows _________ 26
Bayer Group Consolidated Statements of Changes in Equity _________ 27
Notes to the Condensed Consolidated Interim Financial Statements of the Bayer Group __ 28
Events After the End of the Reporting Period ___________ 47
Review Report ______________ 48
Financial Calendar ___________ 49
Masthead _____________ 49

Reporting Principles

The Bayer Interim Report is a quarterly financial report that includes an interim group management report and condensed consolidated interim financial statements and satisfies the requirements of Section 115, Paragraph 2, Nos. 1 and 2, Paragraph 3 and Paragraph 4 of the German Securities Trading Act (WpHG). Bayer has prepared the condensed consolidated interim financial statements according to the International Financial Reporting Standards (IFRS) published by the International Accounting Standards Board (IASB) and endorsed by the European Union (E.U.). The interim group management report should be read in conjunction with our Annual Report 2017, which contains a detailed description of our business operations.

First quarter of 2018

Bayer: Operational business held back by currency effects / Major progress with Monsanto acquisition

  • // Group sales €9.1 billion (Fx & portfolio adj. +2.0%)
  • // EBITDA before special items down year on year at €2.9 billion due to currency effects (Fx adj. level with prior-year quarter)
  • // Sales increase at Pharmaceuticals (Fx & portfolio adj.)
  • // Consumer Health down year on year, as expected
  • // Sales of Crop Science match strong prior-year quarter (Fx & portfolio adj.)
  • // Animal Health raises sales (Fx & portfolio adj.) and earnings
  • // Net income €2.0 billion (–6.2%)
  • // Core earnings per share €2.28 (–1.3%)
  • // European Commission and additional regulators conditionally approve Monsanto acquisition
  • // Currency-adjusted Group outlook for 2018 confirmed

Interim Group Management Report as of March 31, 2018

Economic Position of the Bayer Group

Sales of the Bayer Group increased by 2.0% (Fx & portfolio adj.) to €9.1 billion in the first quarter of 2018. Group EBITDA before special items declined by 5.2% to €2.9 billion. Negative currency effects of around €160 million had a particularly significant impact.

Pharmaceuticals registered an increase in sales that was driven primarily by the continued strong development of our key growth products overall. EBITDA before special items declined, however. Business at Consumer Health receded as expected, particularly in Asia /Pacific. Sales of Crop Science matched the strong level of the prior-year quarter, while EBITDA before special items declined. Animal Health increased sales and earnings.

Key Events

The European Commission conditionally approved Bayer's planned acquisition of Monsanto on March 21, 2018. The conditions cover in particular the divestment of certain Bayer businesses. BASF is the intended purchaser of these assets. Bayer expects the transaction to close in the second quarter of 2018.

In April 2018, the investment company Temasek, Singapore, subscribed to 31 million new shares of Bayer, corresponding to around 3.6% of the increased capital stock, for total gross proceeds of €3 billion.

Changes to the Corporate Structure

In connection with the planned acquisition of Monsanto and in preparation for the future combined business, the structure of the Crop Science segment was adjusted as of January 1, 2018, in line with the internal financial reporting system. In the new structure, all the strategic business entities are organizationally located directly below the Crop Science segment.

1. Overview of Sales, Earnings and Financial Position

1.1 Earnings Performance of the Bayer Group1

First quarter of 2018

Group sales

Group sales in the first quarter of 2018 rose by 2.0% (Fx & portfolio adj.) to €9,138 million (reported: – 5.6%). Germany accounted for €1,040 million of this figure.

Sales of Pharmaceuticals advanced by 2.9% (Fx & portfolio adj.) to €4,075 million. At Consumer Health, sales declined by 2.2% (Fx & portfolio adj.) to €1,409 million. Sales of Crop Science, at €2,861 million (Fx & portfolio adj. – 1.0%), matched the level of the strong prior-year quarter, while business at Animal Health expanded by 3.0% (Fx & portfolio adj.) to €414 million.

1 For definition of alternative performance measures, see Annual Report 2017, A 2.4 "Alternative Performance Measures Used by the Bayer Group."

EBITDA before special items

Group EBITDA before special items was down by 5.2%, at €2,896 million. Negative currency effects held back earnings by around €160 million. EBITDA before special items at Pharmaceuticals declined by 5.8% to €1,415 million. At Consumer Health, EBITDA before special items was significantly lower year on year, at €313 million (– 20.2%). EBITDA before special items at Crop Science declined by 6.5% to €1,042 million, while EBITDA before special items at Animal Health rose by 3.0% to €139 million.

Depreciation and amortization

Depreciation, amortization and impairment losses declined by 11.2% to €508 million in the first quarter of 2018 (Q1 2017: €572 million), in part due to currency effects. This figure comprised €297 million (Q1 2017: €342 million) in amortization and impairments on intangible assets and €211 million (Q1 2017: €230 million) in depreciation and impairments on property, plant and equipment. Impairment losses amounted to €21 million (Q1 2017: €47 million). In the prior-year quarter, impairment losses on intangible assets had included an effect from the discontinuation of the Phase II trial with our cooperation partner Regeneron Pharmaceuticals, Inc.

EBIT and special items

EBIT of the Bayer Group declined by 4.8% to €2,310 million (Q1 2017: €2,427 million), after special charges of €78 million (Q1 2017: €102 million). The special charges consisted primarily of expenses of €61 million in connection with the planned acquisition of Monsanto and of €13 million resulting from efficiency improvement programs. EBIT before special items declined by 5.6% to €2,388 million (Q1 2017: €2,529 million).

In the first quarter of 2018, the following special effects were taken into account in calculating EBIT and EBITDA:

A 1
EBIT EBIT EBITDA EBITDA
Q1 2017 Q1 2018 Q1 2017 Q1 2018
2,529 2,388 3,054 2,896
(36) (1) (3) (1)
(9) (5) (8) (5)
(37) (61) (24) (61)
(20) (11) (20) (11)
(15) (5) (15) (5)
(5) (3) (5) (3)
(3) (3)
(102) (78) (55) (78)
(33)
(5) (4) (5) (4)
(21) (61) (21) (61)
(43) (13) (29) (13)
2,427 2,310 2,999 2,818

For definition see Annual Report 2017, A 2.4 "Alternative Performance Measures Used by the Bayer Group."

Special Items Reconciliation by Functional Costs 1
€ million EBIT
Q1 2017
EBIT
Q1 2018
EBITDA
Q1 2017
EBITDA
Q1 2018
Total special items (102) (78) (55) (78)
of which cost of goods sold (25) (10) (11) (10)
of which selling expenses (1) (2) (1) (2)
of which research and development expenses (36) (3) (3) (3)
of which general administration expenses (35) (58) (35) (58)
of which other operating income / expenses (5) (5) (5) (5)

A 2

Income after income taxes from discontinued operations

Income after income taxes from discontinued operations declined to €8 million (Q1 2017: €564 million) due to the deconsolidation of Covestro in the third quarter of 2017.

Net income

Including a financial result of €130 million (Q1 2017: minus €296 million), income before income taxes was €2,440 million (Q1 2017: €2,131 million). The financial result included a gain of €275 million from the sale of Covestro shares at the beginning of the year and pro-rata income of €80 million from the interest in Covestro accounted for using the equity method. The financial result included €236 million in positive special items (Q1 2017: €35 million in negative special items), primarily in connection with the aforementioned gain from the sale of Covestro shares, which was partially offset by special charges in connection with the planned acquisition of Monsanto.

After income tax expense of €494 million (Q1 2017: €424 million) and adjusting for income from discontinued operations after income taxes and noncontrolling interest, net income for the first quarter of 2018 amounted to €1,954 million (Q1 2017: €2,083 million).

Core earnings per share

Earnings per share (total) declined by 6.3% to €2.24 in the first quarter of 2018 (Q1 2017: €2.39), while core earnings per share from continuing operations decreased by 1.3% to €2.28 (Q1 2017: €2.31).

A 3

Core Earnings per Share1
€ million Q1 2017 Q1 2018
EBIT (as per income statements) 2,427 2,310
Amortization and impairment losses /loss reversals on intangible assets 342 297
Impairment losses /loss reversals on property, plant and equipment,
and accelerated depreciation included in special items
13 7
Special items (other than accelerated depreciation, amortization
and impairment losses /loss reversals)
55 78
Core EBIT 2,837 2,692
Financial result (as per income statements) (296) 130
Special items in the financial result 35 (236)
Income taxes (as per income statements) (424) (494)
Special items in income taxes
Tax effects related to amortization, impairment losses /loss reversals and special items (138) (107)
Income after income taxes attributable to noncontrolling interest
(as per income statements)
2
Above-mentioned adjustments attributable to noncontrolling interest
Core net income from continuing operations 2,016 1,985
Shares
Weighted average number of shares 871,387,808 872,467,808
Core earnings per share from continuing operations 2.31 2.28

1 For definition see Annual Report 2017, A 2.4 "Alternative Performance Measures Used by the Bayer Group."

Personnel expenses and employee numbers

Personnel expenses decreased by 7.5% and totaled €2,438 million (Q1 2017: €2,636 million), in part due to currency effects. As of the closing date, the number of employees in the Bayer Group was largely unchanged year on year, at 100,110 (March 31, 2017: 99,860; + 0.3%).

1.2 Business Development by Segment

Pharmaceuticals

Key Data – Pharmaceuticals

Change %1
€ million Q1 2017 Q1 2018 Reported Fx & p adj.
Sales 4,263 4,075 – 4.4 + 2.9
Change in sales 1
Volume + 7.8% + 5.7%
Price – 0.4% – 2.8%
Currency + 2.2% – 7.1%
Portfolio 0.0% – 0.2%
Reported Fx adj.
Sales by region
Europe / Middle East/Africa 1,606 1,611 + 0.3 + 2.6
North America 1,073 923 – 14.0 – 3.0
Asia /Pacific 1,312 1,303 – 0.7 + 7.7
Latin America 272 238 – 12.5 + 2.6
EBITDA1 1,499 1,414 – 5.7
Special items 1 (3) (1)
EBITDA before special items 1 1,502 1,415 – 5.8
EBITDA margin before special items 1 35.2% 34.7%
EBIT1 1,219 1,163 – 4.6
Special items 1 (36) (1)
EBIT before special items 1 1,255 1,164 – 7.3
Net cash provided by operating activities 973 1,232 + 26.6

A 4

Fx & p adj. = currency- and portfolio-adjusted; Fx adj. = currency-adjusted

1 For definition see Annual Report 2017, A 2.4 "Alternative Performance Measures Used by the Bayer Group."

First quarter of 2018

Sales

Sales of Pharmaceuticals increased by 2.9% (Fx & portfolio adj.) to €4,075 million in the first quarter of 2018. Our key growth products Xarelto™, Eylea™, Xofigo™, Stivarga™ and Adempas™ once again delivered strong performance overall, with their combined sales rising by 14.1% (Fx adj.) to €1,561 million (Q1 2017: €1,445 million). Combined sales of the 15 best-selling Pharmaceuticals products advanced by 5.8% (Fx adj.). We registered a noticeable decline in sales of Kogenate™ that resulted from the termination of an agreement with a distribution partner at the end of 2017. After adjusting for this effect, sales of Pharmaceuticals rose by 4.6% (Fx & portfolio adj.). In addition, temporary supply disruptions for some of our established products had a negative impact on sales, as expected.

Best-Selling Pharmaceuticals Products

A 5

Change %1
€ million Q1 2017 Q1 2018 Reported Fx adj.
Xarelto™ 751 814 + 8.4 + 13.0
of which U.S.A.2 86 83 – 3.5 – 2.7
Eylea™ 446 504 + 13.0 + 19.2
of which U.S.A.3 0 0
Xofigo™ 100 92 – 8.0 + 2.0
of which U.S.A. 62 51 – 17.7 – 3.9
Adempas™ 73 81 + 11.0 + 21.2
of which U.S.A. 38 37 – 2.6 + 14.8
Stivarga™ 75 70 – 6.7 + 3.3
of which U.S.A. 39 29 – 25.6 – 12.3
Subtotal key growth products 1,445 1,561 + 8.0 + 14.1
Mirena™ product family 315 317 + 0.6 + 13.4
of which U.S.A. 219 224 + 2.3 + 18.2
Kogenate™/Kovaltry™ 275 214 – 22.2 – 15.9
of which U.S.A. 94 80 – 14.9 – 1.5
Adalat™ 174 176 + 1.1 + 9.0
of which U.S.A. 0 0
Glucobay™ 158 168 + 6.3 + 13.7
of which U.S.A. 1 0
Nexavar™ 207 162 – 21.7 – 14.3
of which U.S.A. 75 43 – 42.7 – 34.0
YAZ™/Yasmin™/ Yasminelle™ 170 152 – 10.6 – 1.8
of which U.S.A. 20 15 – 25.0 – 13.3
Aspirin™ Cardio 157 148 – 5.7 + 1.1
of which U.S.A. 0 0
Betaferon™/Betaseron™ 171 130 – 24.0 – 16.5
of which U.S.A. 94 58 – 38.3 – 28.8
Avalox™/Avelox™ 100 97 – 3.0 + 3.6
of which U.S.A. 3 3
Gadavist™/Gadovist™ 89 87 – 2.2 + 4.7
of which U.S.A. 27 25 – 7.4 + 6.9
Total best-selling products 3,261 3,212 – 1.5 + 5.8
Proportion of Pharmaceuticals sales 76% 79%
Total best-selling products in U.S.A. 758 648 – 14.5 – 3.4

Fx adj. = currency-adjusted

1 For definition see Annual Report 2017, A 2.4 "Alternative Performance Measures Used by the Bayer Group."

2 Marketing rights owned by a subsidiary of Johnson & Johnson, U.S.A.; transactional effects had a negative impact of €12 million.

3 Marketing rights owned by Regeneron Pharmaceuticals Inc., U.S.A.

Sales by product

// Sales of our oral anticoagulant Xarelto™ increased markedly again, due particularly to expanded volumes in Europe and Asia /Pacific. Our license revenues – recognized as sales – in the United States, where Xarelto™ is marketed by a subsidiary of Johnson & Johnson, were down year on year.

// Business with our eye medicine Eylea™ expanded strongly, primarily due to higher volumes in Europe.

  • // We registered a slight increase in sales of our cancer drug Xofigo™. Higher demand in Japan and Europe more than offset the decline in the United States.
  • // Sales of our pulmonary hypertension treatment Adempas™ rose strongly due primarily to positive development in the United States and Europe and, as in the past, reflected the proportionate recognition of the upfront and milestone payments resulting from the sGC collaboration with Merck & Co., United States.
  • // We posted growth in sales of our cancer drug Stivarga™ that was attributable to expanded volumes in Japan and China, where we benefited from the market launches in previous years. By contrast, sales declined significantly in the United States as a result of competitive pressure.

  • // Sales of the hormone-releasing intrauterine devices of the Mirena™ product family (Mirena™, Kyleena™ and Jaydess™/Skyla™) rose considerably, especially in the United States, where the successful launch of Kyleena™ continued to have a positive impact.

  • // Business with our Kogenate™/Kovaltry™ blood-clotting medicines was negatively impacted by the termination of an agreement with a distribution partner at the end of 2017. Adjusted for this effect, sales climbed 11.1% (Fx adj.).
  • // The marked rise in sales of our diabetes treatment Glucobay™ and of Adalat™, our product for the treatment of hypertension and coronary heart disease, was mainly attributable to the expansion of volumes in China.
  • // We registered a significant decline in sales of our cancer drug Nexavar™ that was mainly the result of lower demand in the United States.
  • // Sales of our YAZ™/Yasmin™/Yasminelle™ line of oral contraceptives moved back, due chiefly to generic competition in Europe and the United States. Business developed positively in Japan and China.
  • // We posted a slight increase in sales of our Aspirin™ Cardio product for the secondary prevention of heart attacks, primarily due to the continuation of our good business performance in China. Slightly lower volumes in Europe had an opposing effect.
  • // Business with our multiple sclerosis product Betaferon™/ Betaseron™ moved back significantly, as expected. This was mainly due to the highly competitive market environment in the United States.
  • // We posted an increase in sales of our antibiotic Avalox™/Avelox™ that resulted particularly from the good development of business in China.
  • // Sales of our MRI contrast agent Gadavist/ Gadovist™ rose, especially in the United States.

Earnings

EBITDA before special items of Pharmaceuticals declined by 5.8% to €1,415 million in the first quarter of 2018 (Q1 2017: €1,502 million). Adjusted for negative currency effects in the amount of €69 million, earnings were down by 1.2%. This decline was driven by a higher cost of goods sold, primarily due to higher project costs in connection with capital expenditures for production facilities, as well as an increase in research and development expenses and higher selling expenses. By contrast, positive earnings contributions primarily came from a significant expansion of volumes, particularly for our key growth products.

EBIT decreased by 4.6% to €1,163 million, after special charges of €1 million (Q1 2017: €36 million).

A 6
Special Items 1
Pharmaceuticals
€ million EBIT
Q1 2017
EBIT
Q1 2018
EBITDA
Q1 2017
EBITDA
Q1 2018
Restructuring (3) (1) (3) (1)
Impairment losses /reversals (33)
Total special items (36) (1) (3) (1)

Consumer Health

Key Data – Consumer Health
Change %1
€ million Q1 2017 Q1 2018 Reported Fx & p adj.
Sales 1,601 1,409 – 12.0 – 2.2
Changes in sales 1
Volume + 0.3% – 3.3%
Price + 2.3% + 1.1%
Currency + 2.7% – 9.8%
Portfolio 0.0% 0.0%
Reported Fx adj.
Sales by region
Europe / Middle East/Africa 538 496 – 7.8 – 3.5
North America 701 596 – 15.0 – 2.1
Asia /Pacific 220 177 – 19.5 – 12.3
Latin America 142 140 – 1.4 + 16.9
EBITDA1 384 308 – 19.8
Special items 1 (8) (5)
EBITDA before special items 1 392 313 – 20.2
EBITDA margin before special items 1 24.5% 22.2%
EBIT1 278 211 – 24.1
Special items 1 (9) (5)
EBIT before special items 1 287 216 – 24.7
Net cash provided by operating activities 265 173 – 34.7

A 7

Fx & p adj. = currency- and portfolio-adjusted; Fx adj. = currency-adjusted

1 For definition see Annual Report 2017, A 2.4 "Alternative Performance Measures Used by the Bayer Group."

First quarter of 2018

Best-Selling Consumer Health Products

Sales

Sales of Consumer Health declined by 2.2% (Fx & portfolio adj.) in the first quarter of 2018 to €1,409 million. This development was driven by the sharp decline in Asia /Pacific that resulted mainly from the reclassification of two of our medicated skin care brands from OTC to prescription by the Chinese authorities in the fall of 2017. Sales also developed negatively in North America and in Europe / Middle East/Africa. In Latin America, by contrast, we posted encouraging sales gains on a currency-adjusted basis.

A 8

Change %1
€ million Q1 2017 Q1 2018 Reported Fx adj.
Claritin™ 190 167 – 12.1 – 0.2
Aspirin™ 117 109 – 6.8 + 3.1
Bepanthen™/Bepanthol™ 95 100 + 5.3 + 10.7
Coppertone™ 102 86 – 15.7 – 3.4
Aleve™ 82 72 – 12.2 + 1.1
Canesten™ 70 52 – 25.7 – 21.2
Alka-Seltzer™ product family 70 52 – 25.7 – 14.5
Elevit™ 52 50 – 3.8 + 6.1
Dr Scholl's™ ² 41 49 19.5 + 34.8
One A Day™ 55 46 – 16.4 – 3.0
Total 874 783 – 10.4 + 0.2
Proportion of Consumer Health sales 55% 56%

Fx adj. = currency-adjusted

For definition see Annual Report 2017, A 2.4 "Alternative Performance Measures Used by the Bayer Group."

2 Trademark rights and distribution only in certain countries outside the European Union

Sales by product

  • // Sales of our antihistamine Claritin™ came in at the prior-year level after adjusting for currency effects. Growth in China offset declines in Japan that arose from intense competitive pressure, as well as negative effects resulting from a slow start to the allergy season in the United States.
  • // Sales of our analgesic Aspirin™ increased, thanks mainly to gains in Latin America. Including business with Aspirin™ Cardio, which is reported under Pharmaceuticals, sales amounted to €257 million (Q1 2017: €274 million), representing currency-adjusted growth of 2.0%.
  • // Business with our Bepanthen™/ Bepanthol™ wound and skin care products developed positively, especially in Brazil and Europe.
  • // Sales of our sunscreen product Coppertone™ declined due to a weaker season, particularly in the United States.
  • // We registered slightly higher sales of our analgesic Aleve™ compared with a weak prior-year quarter, primarily in Brazil and the United States.
  • // Business with our Canesten™ skin and intimate health products receded considerably, due chiefly to anticipated temporary supply disruptions.
  • // We registered a noticeable decline in sales of our Alka-Seltzer™ product family to treat gastric complaints and cold symptoms, due in part to intense competitive pressure.
  • // Sales of our prenatal vitamin Elevit™ continued to expand thanks mainly to good demand in Europe.
  • // Our Dr. Scholl's™ foot care products posted strong sales gains that were attributable particularly to the inventory reduction undertaken in the prior-year quarter in preparation for the repositioning of the brand.
  • // Business with our One A Day™ vitamin product in the United States declined against the prior-year quarter, in which we had benefited from a product line extension.

Earnings

EBITDA before special items of Consumer Health declined by a substantial 20.2% to €313 million in the first quarter of 2018 (Q1 2017: €392 million). Adjusted for negative currency effects in the amount of €34 million, earnings were down by 11.5%. This decline was driven by lower volumes that chiefly resulted from anticipated temporary supply disruptions and the reclassification of two of our brands in China. In the prior-year quarter, earnings had included one-time gains of €34 million. Positive earnings contributions in the first quarter of 2018 predominantly came from a lower cost of goods sold.

EBIT declined by 24.1% to €211 million, after net special charges of €5 million (Q1 2017: €9 million) resulting from efficiency improvement measures.

A 9
Special Items 1
Consumer Health
€ million EBIT
Q1 2017
EBIT
Q1 2018
EBITDA
Q1 2017
EBITDA
Q1 2018
Restructuring (9) (5) (8) (5)
Total special items (9) (5) (8) (5)

Crop Science

Key Data – Crop Science
Change % 1
€ million Q1 2017 Q1 2018 Reported Fx & p adj.
Sales 3,120 2,861 – 8.3 – 1.0
Change in sales 1
Volume + 3.4% – 0.6%
Price – 0.2% – 0.4%
Currency + 3.1% – 7.3%
Portfolio 0.0% 0.0%
Reported Fx adj.
Sales by region
Europe / Middle East/Africa 1,462 1,294 – 11.5 – 8.8
North America 1,042 969 – 7.0 + 4.5
Asia /Pacific 366 368 + 0.5 + 10.4
Latin America 250 230 – 8.0 + 4.8
EBITDA1 1,091 981 – 10.1
Special items 1 (24) (61)
EBITDA before special items 1 1,115 1,042 – 6.5
EBITDA margin before special items 1 35.7% 36.4%
EBIT1 970 892 – 8.0
Special items 1 (37) (61)
EBIT before special items 1 1,007 953 – 5.4
Net cash used in operating activities (679) (703) – 3.5

A 10

Fx & p adj. = currency- and portfolio-adjusted; Fx adj. = currency-adjusted

1 For definition see Annual Report 2017, A 2.4 "Alternative Performance Measures Used by the Bayer Group."

First quarter of 2018

Sales

In the first quarter of 2018, Crop Science posted sales of €2,861 million (Fx & portfolio adj. – 1.0%), which was level with the strong prior-year quarter. Sales declines in Europe / Middle East/Africa were nearly offset by gains in North America, Asia /Pacific and Latin America.

A 11
Sales by Business Unit Change %1
€ million Q1 2017 Q1 2018 Reported Fx & p
adj.
Crop Science 3,120 2,861 – 8.3 – 1.0
Herbicides 912 800 – 12.3 – 6.6
Fungicides 787 728 – 7.5 – 2.0
Insecticides 301 299 – 0.7 + 8.0
SeedGrowth 251 210 – 16.3 – 8.4
Vegetable Seeds 162 144 – 11.1 – 6.2
Environmental Science 147 114 – 22.4 – 14.3
Other (Seeds & Traits) 560 566 + 1.1 + 12.9

Fx & p adj. = currency- and portfolio-adjusted

Sales by region

  • // Sales in the Europe / Middle East/Africa region fell by 8.8% (Fx adj.) to €1,294 million. We recorded lower sales at Fungicides, Herbicides and Vegetable Seeds, mainly due to the weather conditions in Europe. At Fungicides, business was also held back by a substantial market decline in France. Sales at SeedGrowth were also down year on year. In contrast, sales increased at Insecticides, but this growth was insufficient to offset the declines elsewhere.
  • // Sales in North America advanced by 4.5% (Fx adj.) to €969 million. The canola seed business in Canada performed very well due to increased acreages. Higher demand in Canada resulted in sales gains at Herbicides. On the other hand, there was a significant decline at Environmental Science due to lower product deliveries to the purchaser of our consumer business and at Insecticides due to lower pest pressure in the United States.
  • // In the Asia /Pacific region, sales increased by 10.4% (Fx adj.) to €368 million. The encouraging growth at Fungicides and Insecticides was attributable especially to advance sales in China and to high pest pressure in India. By contrast, sales were down at Herbicides.
  • // In Latin America, sales advanced by 4.8% (Fx adj.) to €230 million. We posted double-digit percentage growth at Fungicides after a weak prior-year quarter. In Brazil, demand for our fungicides and insecticides increased, while inventories continued to normalize. However, sales at Herbicides declined, especially in Argentina.

Earnings

EBITDA before special items of Crop Science decreased by 6.5% to €1,042 million in the first quarter of 2018 (Q1 2017: €1,115 million). Adjusted for negative currency effects in the amount of €44 million, earnings were down by 2.6%. A decline in other operating income and a higher cost of goods sold were among factors that held back earnings. Lower expenses for research and development and for general administration had an opposing effect.

EBIT declined by 8.0% to €892 million, after special charges of €61 million (Q1 2017: €37 million), primarily in connection with the planned acquisition of Monsanto.

A 12
Special Items 1
Crop Science
€ million EBIT
Q1 2017
EBIT
Q1 2018
EBITDA
Q1 2017
EBITDA
Q1 2018
Restructuring (16) (2) (3) (2)
Litigations (1) (1)
Acquisition costs (21) (58) (21) (58)
Total special items (37) (61) (24) (61)

A 13

Animal Health

Change %1
Q1 2017 Q1 2018 Reported Fx & p adj.
440 414 – 5.9 + 3.0
– 0.3% + 2.5%
+ 3.2% + 0.5%
+ 3.1% – 8.9%
+ 1.8% 0.0%
Reported Fx adj.
144 136 – 5.6 – 4.2
177 160 – 9.6 + 4.5
76 77 + 1.3 + 11.8
43 41 – 4.7 + 7.0
135 139 + 3.0
135 139 + 3.0
30.7% 33.6%
126 129 + 2.4
126 129 + 2.4
(31) 13

Fx & p adj. = currency- and portfolio-adjusted; Fx adj. = currency-adjusted

1 For definition see Annual Report 2017, A 2.4 "Alternative Performance Measures Used by the Bayer Group."

First quarter of 2018

Sales

Sales of Animal Health in the first quarter of 2018 increased by 3.0% (Fx & portfolio adj.) to €414 million. Growth was negatively impacted by amended financial reporting standards (IFRS 15), among other factors. The Asia /Pacific region developed very positively. We also expanded business in Latin and North America on a currency-adjusted basis, while sales receded in Europe / Middle East/Africa.

A 14

Best-Selling Animal Health Products
Change %1
€ million Q1 2017 Q1 2018 Reported Fx adj.
Advantage™ product family 136 114 – 16.2 – 8.2
Seresto™ 76 88 + 15.8 + 24.8
Drontal™ product family 35 31 – 11.4 – 4.4
Baytril™ 27 25 – 7.4 + 2.9
Total 274 258 – 5.8 + 2.6
Proportion of Animal Health sales 62% 62%

Fx adj. = currency-adjusted

1 For definition see Annual Report 2017, A 2.4 "Alternative Performance Measures Used by the Bayer Group."

Sales by product

// Business with our Advantage™ line of flea, tick and worm control products decreased in the Europe / Middle East/Africa and North America regions due to seasonal shifts. Volumes in North America were also negatively impacted by increased competitive pressure and the related decline in demand. Growth in Asia /Pacific was not sufficient to offset this development.

  • // Business with our Seresto™ flea and tick collar once again clearly expanded in all regions. This development was mainly driven by higher demand in the United States and by price and volume increases in the Europe / Middle East/Africa region.
  • // We registered lower volumes of our Drontal™ line of dewormers in the Europe / Middle East/Africa region. In addition, demand in North America was below that of the strong prior-year quarter.
  • // There was a slight increase in sales of our Baytril™ antibiotic. Here we benefited from positive business development in the North America, Asia /Pacific and Latin America regions.

Earnings

EBITDA before special items of Animal Health increased by 3.0% to €139 million in the first quarter of 2018 (Q1 2017: €135 million). Adjusted for negative currency effects in the amount of €10 million, earnings were up by 10.4%. Positive contributions came from lower selling expenses, while the aforementioned effect of the first-time application of IFRS 15 had a negative impact on earnings.

EBIT improved by 2.4% to €129 million. As in the prior-year quarter, it included no special items.

1.3 Asset and Financial Position of the Bayer Group

Statement of Cash Flows

Q1 2017 Q1 2018 Change %
551 658 + 19.4
290 – 100.0
841 658 – 21.8
(1,136) (2,058) – 81.2
611 (581)
316 (1,981)
1,899 7,436
9 (117)
2,224 5,338 + 140.0

A 15

2017 figures restated

Net cash provided by operating activities

// In the first quarter of 2018, the net cash provided by operating activities (total) declined by 21.8% to €658 million. Covestro was still included in the prior-year quarter. The net cash provided by operating activities in continuing operations rose by 19.4% to €658 million due mainly to lower additions to cash tied up in working capital.

Net cash used in investing activities

  • // Cash outflows for property, plant and equipment and intangible assets were 15.9% lower in the first quarter of 2018 at €349 million (Q1 2017: €415 million), and included €219 million (Q1 2017: €152 million) at Pharmaceuticals, €28 million (Q1 2017: €24 million) at Consumer Health, €63 million (Q1 2017: €99 million) at Crop Science and €5 million (Q1 2017: €6 million) at Animal Health. The prioryear figures included €74 million at Covestro.
  • // There was a net cash inflow of €1,802 million from the sale of further Covestro shares.
  • // We invested €3,712 million in current financial assets (Q1 2017: €583 million).

Net cash used in financing activities

  • // In the first quarter of 2018, there was a net cash outflow of €581 million for financing activities, including net loan repayments of €507 million (Q1 2017: €744 million).
  • // The prior-year-quarter figure included a net inflow of €1,460 million from the sale of Covestro shares while that company remained fully consolidated.
  • // Net interest payments decreased by €31 million to €74 million.

Liquid assets and net financial debt

A 16
Net Financial Debt 1
€ million Dec. 31,
2017
March 31,
2018
Change
(%)
Bonds and notes /promissory notes 12,436 12,290 – 1.2
of which hybrid bonds 2 4,533 4,534
Liabilities to banks 534 611 + 14.4
Liabilities under finance leases 238 248 + 4.2
Liabilities from derivatives 3 240 199 – 17.1
Other financial liabilities 970 686 – 29.3
Receivables from derivatives 3 (244) (223) – 8.6
Financial debt 14,174 13,811 – 2.6
Cash and cash equivalents (7,581) (5,332) – 29.7
Current financial assets 4 (2,998) (6,829) + 127.8
Net financial debt 3,595 1,650 – 54.1
1
For definition see Annual Report 2017, A 2.4 "Alternative Performance Measures Used by the Bayer Group."

2

Classified as debt according to IFRS 3 These include the market values of interest-rate and currency hedges of recorded transactions.

4 These include short-term loans and receivables with maturities between 3 and 12 months outstanding from banks and other companies as well as financial investments in debt and equity instruments that were recorded as current on first-time recognition.

// Net financial debt of the Bayer Group decreased to €1.7 billion between December 31, 2017, and the end of the first quarter, due mainly to cash inflows from the sale of further Covestro shares.

// Net financial debt includes three subordinated hybrid bonds with a total volume of €4.5 billion, 50% of which is treated as equity by Moody's and S & P Global Ratings. The hybrid bonds thus have a more limited effect on the Group's rating-specific debt indicators than senior debt.

// The other financial liabilities as of March 31, 2018, contained €528 million related to the mandatory convertible notes issued in November 2016.

// S & P Global Ratings and Moody's give Bayer long-term issuer ratings of A– and A3, respectively. The short-term ratings are A–2 (S & P Global Ratings) and P–2 (Moody's). These investment-grade ratings demonstrate good creditworthiness. In connection with the planned acquisition of Monsanto, both rating agencies are currently reviewing the long-term issuer ratings with regard to a potential downgrade. In addition, Moody's is currently reviewing its short-term P–2 rating.

Asset and capital structure

Bayer Group Summary Statements of Financial Position
------------------------------------------------------ -- -- -- -- --
€ million Dec. 31,
2017
March 31,
2018
Change %
Noncurrent assets 45,014 42,225 – 6.2
Assets held for sale 2,081 3,132 + 50.5
Other current assets 27,992 30,037 + 7.3
Current assets 30,073 33,169 + 10.3
Total assets 75,087 75,394 + 0.4
Equity 36,861 38,384 + 4.1
Noncurrent liabilities 24,633 23,912 – 2.9
Liabilities directly related to assets held for sale 111 520
Other current liabilities 13,482 12,578 – 6.7
Current liabilities 13,593 13,098 – 3.6
Liabilities 38,226 37,010 – 3.2
Total equity and liabilities 75,087 75,394 + 0.4

// Between December 31, 2017, and March 31, 2018, total assets increased by €0.3 billion to €75.4 billion.

  • // Noncurrent assets decreased by €2.8 billion to €42.2 billion. Investments accounted for using the equity method declined by €1.4 billion, largely through the sale of further Covestro shares. Total current assets increased by €3.1 billion to €33.2 billion. The assets held for sale in connection with the planned acquisition of Monsanto increased by €1.1 billion, due particularly to the planned sale of the vegetable seeds business.
  • // Equity rose by €1.5 billion compared with December 31, 2017, to €38.4 billion. The income after income taxes of €2.0 billion had a positive effect. Currency effects recognized outside profit and loss reduced equity by €0.4 billion. A decline of €0.2 billion came from the increase in pension provisions outside profit or loss. The equity ratio increased to 50.9% as of March 31, 2018 (March 31, 2017: 49.1%).
  • // Liabilities as of March 31, 2018, decreased by €1.2 billion to €37.0 billion.

2. Research, Development, Innovation

Bayer Group expenses for research and development amounted to €1,040 million in the first quarter of 2018, matching the prior-year level (Fx adj. +0.0%).

Research and Development Expenses
R&D expenses R&D expenses before special items
Change % Change %
€ million Q1 2017 Q1 2018 Fx adj. Q1 2017 Q1 2018 Fx adj.
Pharmaceuticals 712 693 + 1.8 679 693 + 6.8
Consumer Health 59 55 + 1.9 57 55 + 5.4
Crop Science 283 257 – 3.7 282 254 – 4.4
Animal Health 33 30 – 3.6 33 30 – 4.2
Reconciliation 7 5 – 40.0 7 5 – 40.0
Total Group 1,094 1,040 0.0 1,058 1,037 + 3.1

A 18

Pharmaceuticals

We are conducting clinical trials with several drug candidates from our research and development pipeline.

A 19

The following table shows our most important drug candidates currently in Phase II of clinical testing:

Research and Development Projects (Phase II) 1
------------------------------------------------ -- --
Projects Indication
Anetumab ravtansine (mesothelin ADC) Malignant pleural mesothelioma 2
BAY 1128688 (AKR1C3 inhibitor) Endometriosis
Fulacimstat (BAY 1142524, chymase inhibitor) Heart failure
Fulacimstat (BAY 1142524, chymase inhibitor) Chronic kidney disease
BAY 1193397 (AR alpha 2c rec ant.) Peripheral artery disease (PAD)
BAY 1213790 (anti-FXIa antibody) Prevention of thrombosis
BAY 2306001 (IONIS-FXIRx) Prevention of thrombosis 3
Neladenoson bialanate Chronic heart failure
Nesvacumab (Ang2 antibody) + aflibercept Serious eye diseases 4
Radium-223 dichloride Breast cancer with bone metastases
Radium-223 dichloride Multiple myeloma
Riociguat Systemic sclerosis
Vilaprisan (S-PRM) Endometriosis

As of April 5, 2018

2 This trial did not meet its primary endpoint. However, it has not yet been terminated. Additional studies investigating anetumab ravtansine as a treatment for different forms of solid tumors are ongoing. See the Bayer Annual Report 2017 for more information.

3 Sponsored by Ionis Pharmaceuticals, Inc.

4 Sponsored by Regeneron Pharmaceuticals, Inc.

The nature of drug discovery and development is such that not all compounds can be expected to meet the predefined project goals. It is possible that any or all of the projects listed above may have to be discontinued due to scientific and / or commercial reasons and will not result in commercialized products. It is also possible that the requisite U.S. Food and Drug Administration (FDA), European Medicines Agency (EMA) or other regulatory approvals will not be granted for these compounds. Moreover, we regularly review our research and development pipeline so that we can give priority to advancing the most promising pharmaceuticals projects.

The Phase II study with copanlisib in patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL), an aggressive form of non-Hodgkin lymphoma (NHL), was concluded. The results were presented at ASCO 2017 (American Society of Clinical Oncology). A Phase III study in this indication is not currently planned. Bayer continues to investigate copanlisib in a Phase III program pertaining to indolent NHL. The following table shows our most important drug candidates currently in Phase III of clinical testing:

A 20
Research and Development Projects (Phase III) 1
Projects Indication
Copanlisib (PI3K inhibitor) Various forms of non-Hodgkin lymphoma (NHL)
Darolutamide (ODM-201, AR antagonist) Castration-resistant nonmetastatic prostate cancer
Darolutamide (ODM-201, AR antagonist) Hormone-sensitive metastatic prostate cancer
Finerenone (MR antagonist) Diabetic kidney disease
Molidustat (HIF-PH inhibitor) Renal anemia
Radium-223 dichloride Combination treatment of castration-resistant prostate cancer 2
Rivaroxaban Anticoagulation in patients with chronic heart failure 3
Rivaroxaban Prevention of venous thromboembolism in high-risk patients after
discharge from hospital 3
Rivaroxaban Peripheral artery disease (PAD)
Rivaroxaban VTE treatment in children
Vericiguat (sGC stimulator) Chronic heart failure 4
Vilaprisan (S-PRM) Symptomatic uterine fibroids

1 As of April 5, 2018

2 This trial was unblinded ahead of schedule and there are no patients who are still receiving the combination therapy. Otherwise, however, the trial is continuing, especially with regard to per protocol patient monitoring. The final assessment has not yet been completed. For more information see the Bayer Annual Report 2017.

3 Sponsored by Janssen Research & Development, LLC

4 Sponsored by Merck & Co., Inc., USA

The nature of drug discovery and development is such that not all compounds can be expected to meet the predefined project goals. It is possible that any or all of the projects listed above may have to be discontinued due to scientific and / or commercial reasons and will not result in commercialized products. It is also possible that the requisite U.S. Food and Drug Administration (FDA), European Medicines Agency (EMA) or other regulatory approvals will not be granted for these compounds. Moreover, we regularly review our research and development pipeline so that we can give priority to advancing the most promising pharmaceuticals projects.

Bayer and the U.S. study network NSABP (National Surgical Adjuvant Breast and Bowel Project) decided to discontinue ahead of schedule a clinical Phase III study investigating the active substance regorafenib as an adjuvant therapy in colon carcinoma due to an insufficient number of participants.

In March 2018, Bayer and MSD International GmbH, a Group company of Merck & Co., Inc., decided to discontinue the joint development and commercialization of Sivextro™ (active ingredient: tedizolid phosphate) to treat infections of the skin and subcutaneous tissue. Bayer had inlicensed Sivextro™ in July 2011 for emerging markets and Japan. MSD will now continue to develop and market Sivextro™ in a number of these countries.

The most important drug candidates in the approval process are:

A 21

Main Products Submitted for Approval 1

Projects Indication
Damoctocog alpha pegol
(long-acting rFVIII)
Europe, U.S.A., Japan: hemophilia A
Rivaroxaban Europe, U.S.A.: prevention of major adverse cardiac events (MACE),
COMPASS trial
Rivaroxaban 2 U.S.A.: secondary prophylaxis of acute coronary syndrome (ACS),
rivaroxaban in combination with dual antiplatelet therapy (DAPT),
ATLAS trial
Larotrectinib (LOXO-101, TRK inhibitor) 3 Solid tumors with NTRK gene fusions

1 As of April 5, 2018

2 Submitted by Janssen Research & Development, LLC

3 Submitted by Loxo Oncology, Inc.

In February 2018, Eylea™ (active ingredient: aflibercept solution for injection into the eye) was approved by the China Food and Drug Administration (CFDA) for the treatment of visual impairment due to diabetic macular edema. This is the first indication for which Eylea™ has obtained CFDA approval.

In March 2018, Bayer's cooperation partner Loxo Oncology, Inc., Stamford, Connecticut, United States, completed the submission of a rolling New Drug Application (NDA) for larotrectinib in the United States. The registration application refers to the treatment of cancer patients suffering from locally advanced or metastatic solid tumors with neurotrophic tyrosine receptor kinase (NTRK) gene fusions. The active substance larotrectinib was designed to specifically block the signaling pathway responsible for tumor growth.

Crop Science

In February 2018, Bayer and Mitsui Chemicals Agro, Inc. (MCAG), headquartered in Tokyo, Japan, signed a license agreement granting Bayer an exclusive right to develop and commercialize the new fungicide quinofumelin worldwide except in certain selected countries. This product features a broad spectrum of action and is intended particularly for application in fruit tree crops, vegetables, oilseed rape / canola and rice.

At the beginning of March 2018, Bayer and the International Rice Research Institute (IRRI), headquartered in Los Baños, Philippines, signed an agreement confirming Bayer's participation in the Direct Seeded Rice Consortium (DSRC) led by IRRI to drive forward modern rice cultivation technologies in Asia.

Also in March 2018, Bayer, Exeter University in the United Kingdom and Rothamsted Research, headquartered in Harpenden, United Kingdom, identified in a joint study enzymes in honey bees and bumble bees that determine how sensitively they react to different neonicotinoid insecticides. Bayer is convinced the research results will help to selectively develop additional bee-friendly insecticides.

3. Report on Future Perspectives and on Opportunities and Risks

3.1 Future Perspectives

3.1.1 Economic Outlook

Economic Outlook1 A 22
Growth
2017
Growth
forecast
2018
World + 3.3% + 3.4%
European Union + 2.5% + 2.3%
of which Germany + 2.5% + 2.6%
United States + 2.3% + 2.7%
Emerging Markets 2 + 4.8% + 4.9%

2017 figures restated

1 Real growth of gross domestic product, source: IHS Markit

2 Including about 50 countries defined by IHS Markit as Emerging Markets in line with the World Bank

As of April 2018

The global economy should continue to grow in 2018. Although the risks for the world economy have increased in view of growing political tensions, the recent tax cuts in the United States should stimulate growth, and we also anticipate robust growth in Europe in 2018. As for the Emerging Markets, we expect growth in economic output to match the pace of the prior year, while for China, we anticipate continuing strong growth at a slightly slower rate.

Economic Outlook for the Segments1

Growth
2017
Growth
forecast
2018
Pharmaceuticals market + 3% + 4%
Consumer health market + 3 – 4% + 3 – 4%
Seed and crop protection market + 1% + 3%
Animal health market + 2% + 4%

2017 figures restated 1 Bayer's estimate, except pharmaceuticals. Source for pharmaceuticals market: IQVIA Market Prognosis (March 2018); all rights reserved; currency-adjusted

As of March 2018

3.1.2 Corporate Outlook

Based on the business development described in this report and taking into account the potential risks and opportunities, we confirm the currency-adjusted forecasts published in February for operating performance (see Annual Report 2017, A 3.1.2). We continue to expect 2018 sales to increase by a low- to midsingle-digit percentage on a currency- and portfolio-adjusted basis. As before, we aim to increase EBITDA before special items and core earnings per share by a mid-single-digit percentage on a currency-adjusted basis.

Taking into account the exchange rates as at March 31, 2018, reported sales would decline in 2018 overall by a low-single-digit percentage (previously: remain at the prior-year level). In absolute terms, sales would now come in at below €35 billion (previously: around €35 billion). EBITDA before special items would decline by a low-single-digit percentage (previously: match the prior-year level). Core earnings per share would come in at the prior-year level, as previously forecast.

3.2 Opportunities and Risks

As a global enterprise with a diversified portfolio, the Bayer Group is exposed to a wide range of internal or external developments or events that could significantly impact the achievement of our financial and nonfinancial objectives.

Bayer regards opportunity and risk management as an integral part of corporate governance. Our risk management process and the opportunities /risks are outlined in detail in the Annual Report 2017 (Combined Management Report, A 3.2 "Opportunity and Risk Report"). With regard to the risks related to the acquisition of Monsanto Company, United States, we refer specifically to A 3.2.3 "Opportunities and Risks Related to the Planned Acquisition of Monsanto."

There have been no material changes to Bayer's overall risk profile so far compared with our commentary in the Annual Report 2017.

No risks have been identified that could endanger the Bayer Group's continued existence. There are also no risks with mutually reinforcing dependencies that could combine to endanger the Group's continued existence.

Significant developments that have occurred in respect of the legal risks since publication of the Bayer Annual Report 2017 (Note [32] to the Consolidated Financial Statements) are described in the Notes to the Condensed Consolidated Interim Financial Statements under "Legal Risks."

Condensed Consolidated Interim Financial Statements as of March 31, 2018

Bayer Group Consolidated Income Statements

B 1
€ million Q1 2017 Q1 2018
Net sales 9,680 9,138
Cost of goods sold (2,987) (2,909)
Gross profit 6,693 6,229
Selling expenses (2,667) (2,509)
Research and development expenses (1,094) (1,040)
General administration expenses (460) (427)
Other operating income 159 152
Other operating expenses (204) (95)
EBIT1 2,427 2,310
Equity-method income (loss) (7) 71
Financial income 32 370
Financial expenses (321) (311)
Financial result (296) 130
Income before income taxes 2,131 2,440
Income taxes (424) (494)
Income from continuing operations after income taxes 1,707 1,946
of which attributable to noncontrolling interest (2)
of which attributable to Bayer AG stockholders (net income) 1,709 1,946
Income from discontinued operations after income taxes 564 8
of which attributable to noncontrolling interest 190
of which attributable to Bayer AG stockholders (net income) 374 8
Income after income taxes 2,271 1,954
of which attributable to noncontrolling interest 188
of which attributable to Bayer AG stockholders (net income) 2,083 1,954
Earnings per share
From continuing operations
Basic 1.96 2.23
Diluted 1.96 2.23
From discontinued operations
Basic 0.43 0.01
Diluted 0.43 0.01
From continuing and discontinued operations
Basic 2.39 2.24
Diluted 2.39 2.24

2017 figures restated

Bayer Group Consolidated Statements of Comprehensive Income

B 2
€ million Q1 2017 Q1 2018
Income after income taxes 2,271 1,954
of which attributable to noncontrolling interest 188
of which attributable to Bayer AG stockholders 2,083 1,954
Remeasurements of the net defined benefit liability for post-employment benefit plans 605 (176)
Income taxes (195) (1)
Other comprehensive income from remeasurements of the net defined benefit liability
for post-employment benefit plans
410 (177)
Changes in fair values of equity instruments measured at fair value through other
comprehensive income
95
Income taxes
Other comprehensive income from equity instruments measured at fair value through
other comprehensive income
95
Other comprehensive income relating to associates accounted for using
the equity method
(13)
Other comprehensive income that will not be reclassified subsequently to profit or loss 410 (95)
Changes in fair values of cash flow hedges (88) 60
Reclassified to profit or loss 54 (31)
Income taxes 15 (8)
Other comprehensive income from cash flow hedges (19) 21
Changes in fair values of available-for-sale financial assets (7)
Reclassified to profit or loss
Income taxes 9
Other comprehensive income from available-for-sale financial assets 2
Changes in exchange differences recognized on translation of operations
outside the eurozone
(171) (382)
Reclassified to profit or loss
Other comprehensive income from exchange differences (171) (382)
Other comprehensive income relating to associates accounted for using
the equity method
7 (1)
Other comprehensive income that may be reclassified subsequently to profit or loss (181) (362)
Total other comprehensive income 1 229 (457)
of which attributable to noncontrolling interest 23 (4)
of which attributable to Bayer AG stockholders 206 (453)
Total comprehensive income 2,500 1,497
of which attributable to noncontrolling interest 211 (4)
of which attributable to Bayer AG stockholders 2,289 1,501

Total changes recognized outside profit or loss

Bayer Group Consolidated Statements of Financial Position

March 31, March 31, Dec. 31,
€ million 2017 2018 2017
Noncurrent assets
Goodwill 16,290 14,480 14,751
Other intangible assets 13,367 11,185 11,674
Property, plant and equipment 13,085 7,330 7,633
Investments accounted for using the equity method 580 2,574 4,007
Other financial assets 1,308 1,737 1,634
Other receivables 568 535 400
Deferred taxes 6,466 4,384 4,915
51,664 42,225 45,014
Current assets
Inventories 8,674 6,402 6,550
Trade accounts receivable 13,020 9,498 8,582
Other financial assets 6,662 7,315 3,529
Other receivables 2,205 1,029 1,276
Claims for income tax refunds 577 461 474
Cash and cash equivalents 2,224 5,332 7,581
Assets held for sale 28 3,132 2,081
33,390 33,169 30,073
Total assets 85,054 75,394 75,087
Equity
Capital stock 2,117 2,117 2,117
Capital reserves 9,658 9,658 9,658
Other reserves 21,842 26,553 25,026
Equity attributable to Bayer AG stockholders 33,617 38,328 36,801
Equity attributable to noncontrolling interest 2,240 56 60
35,857 38,384 36,861
Noncurrent liabilities
Provisions for pensions and other post-employment benefits 10,522 8,096 8,020
Other provisions 1,753 1,302 1,366
Refund liabilities 146
Contract liabilities 799
Financial liabilities 14,788 12,273 12,483
Income tax liabilities 204 482 495
Other liabilities 933 228 1,116
Deferred taxes 1,425 586 1,153
29,625 23,912 24,633
Current liabilities
Other provisions 6,130 2,194 4,344
Refund liabilities 2,519
Contract liabilities 197
Financial liabilities 4,199 1,761 1,935
Trade accounts payable 5,690 3,943 5,129
Income tax liabilities 1,307 646 422
Other liabilities 2,246 1,318 1,652
Liabilities directly related to assets held for sale 520 111
19,572 13,098 13,593
Total equity and liabilities 85,054 75,394 75,087

B 3

Bayer Group Consolidated Statements of Cash Flows

€ million Q1 2017 Q1 2018
Income from continuing operations after income taxes 1,707 1,946
Income taxes 424 494
Financial result 296 (130)
Income taxes paid (493) (388)
Depreciation, amortization and impairments 572 508
Change in pension provisions (63) (98)
(Gains) losses on retirements of noncurrent assets (50) (20)
Decrease (increase) in inventories (100) (84)
Decrease (increase) in trade accounts receivable (1,645) (1,349)
(Decrease) increase in trade accounts payable (728) (436)
Changes in other working capital, other noncash items 631 215
Net cash provided by (used in) operating activities from continuing operations 551 658
Net cash provided by (used in) operating activities from
discontinued operations
290
Net cash provided by (used in) operating activities (total) 841 658
Cash outflows for additions to property, plant, equipment and intangible assets (415) (349)
Cash inflows from the sale of property, plant, equipment and other assets 54 59
Cash inflows from divestments 145
Cash inflows from (outflows for) noncurrent financial assets (54) 1,777
Cash outflows for acquisitions less acquired cash (158)
Interest and dividends received 20 22
Cash inflows from (outflows for) current financial assets (583) (3,712)
Net cash provided by (used in) investing activities (total) (1,136) (2,058)
Proceeds from shares of Covestro AG 1,460
Dividend payments
Issuances of debt 292 1,021
Retirements of debt (1,036) (1,528)
Interest paid including interest-rate swaps (114) (83)
Interest received from interest-rate swaps 9 9
Cash outflows for the purchase of additional interests in subsidiaries
Net cash provided by (used in) financing activities (total) 611 (581)
Change in cash and cash equivalents due to business activities (total) 316 (1,981)
Cash and cash equivalents at beginning of period 1,899 7,436
Change in cash and cash equivalents due to changes in scope of consolidation 1
Change in cash and cash equivalents due to exchange rate movements 9 (118)
Cash and cash equivalents at end of period 2,224 5,338

2017 figures restated

Bayer Group Consolidated Statements of Changes in Equity

€ million Capital stock Capital
reserves
Other
reserves
Equity
attributable
to Bayer AG
stockholders
Equity
attributable
to non
controlling
interest
Equity
Dec. 31, 2016 2,117 9,658 18,558 30,333 1,564 31,897
Equity transactions with owners
Capital increase / decrease
Dividend payments
Other changes 995 995 465 1,460
Total comprehensive income 2,289 2,289 211 2,500
March 31, 2017 2,117 9,658 21,842 33,617 2,240 35,857
Dec. 31, 2017 2,117 9,658 25,026 36,801 60 36,861
Adjustment on adoption of
IFRS 9 (net of tax)
(60) (60) (60)
Adjustment on adoption of
IFRS 15 (net of tax)
86 86 86
Equity transactions with owners
Capital increase / decrease
Dividend payments
Other changes
Total comprehensive income 1,501 1,501 (4) 1,497
March 31, 2018 2,117 9,658 26,553 38,328 56 38,384

B 5

Notes to the Condensed Consolidated Interim Financial Statements of the Bayer Group

B 6

Key Data by Segment

Key Data by Segment

Pharmaceuticals Consumer Health Crop Science Animal Health
€ million Q1 2017 Q1 2018 Q1 2017 Q1 2018 Q1 2017 Q1 2018 Q1 2017 Q1 2018
Net sales (external) 4,263 4,075 1,601 1,409 3,120 2,861 440 414
Change 1 + 9.6% – 4.4% + 5.3% – 12.0% + 6.3% – 8.3% + 7.8% – 5.9%
Currency-adjusted change 1 + 7.4% + 2.7% + 2.6% – 2.2% + 3.2% – 1.0% + 4.7% + 3.0%
Intersegment sales 10 9 5 1 8 8 1 2
Net sales (total) 4,273 4,084 1,606 1,410 3,128 2,869 441 416
EBIT1 1,219 1,163 278 211 970 892 126 129
EBIT before special items 1 1,255 1,164 287 216 1,007 953 126 129
EBITDA before special items 1 1,502 1,415 392 313 1,115 1,042 135 139
Net cash provided
by operating activities
973 1,232 265 173 (679) (703) (31) 13
Depreciation, amortization,
impairment losses /loss reversals
280 251 106 97 121 89 9 10
1

For definition see Annual Report 2017, A 2.4 "Alternative Performance Measures Used by the Bayer Group."

B 6 continued

Key Data by Segment

Group
All Other Segments Corporate Functions
and Consolidation
€ million Q1 2017 Q1 2018 Q1 2017 Q1 2018 Q1 2017 Q1 2018
Net sales (external) 252 378 4 1 9,680 9,138
Change 1 + 0.8% + 50.0% + 7.5% – 5.6%
Currency-adjusted change 1 + 2.0% + 48.0% + 5.0% + 1.9%
Intersegment sales 710 595 (734) (615)
Net sales (total) 962 973 (730) (614) 9,680 9,138
EBIT1 (26) 22 (140) (107) 2,427 2,310
EBIT before special items 1 (8) 30 (138) (104) 2,529 2,388
EBITDA before special items 1 45 87 (135) (100) 3,054 2,896
Net cash provided
by operating activities
(167) (243) 190 186 551 658
Depreciation, amortization,
impairment losses /loss reversals
53 57 3 4 572 508

2017 figures restated

Explanatory Notes

Accounting policies

The consolidated interim financial statements as of March 31, 2018, were prepared in condensed form in compliance with IAS 34 according to the International Financial Reporting Standards (IFRS) of the International Accounting Standards Board (IASB), London, which are endorsed by the European Union, and the Interpretations of the IFRS Interpretations Committee in effect at the closing date.

Reference should be made as appropriate to the Notes to the Consolidated Financial Statements for the 2017 fiscal year, particularly with regard to the main recognition and measurement principles, except where financial reporting standards have been applied for the first time in 2018 or an accounting policy has changed.

Financial reporting standards applied for the first time in 2018

IFRS 9 (Financial Instruments) and IFRS 15 (Revenue from Contracts with Customers) were applied for the first time as of January 1, 2018. The effects resulting from their first-time application are detailed in this section.

IFRS 9 is the new standard for accounting for financial instruments that Bayer applied retrospectively for the first time as of January 1, 2018, without restating the prior-year figures, accounting for the aggregate amount of any transition effects by way of an adjustment to equity and presenting the comparative period in line with previous rules.

The effects that the first-time application of IFRS 9 and IFRS 15 had on retained earnings and other comprehensive income in the statement of comprehensive income are detailed in the following tables:

B 7

Retained Earnings Reconciliation: IFRS 9 and IFRS 15

€ million
Retained earnings incl. net income as at December 31, 2017 26,851
Effects of IFRS 9 (43)
of which reclassification from other comprehensive income (fair-value measurement of financial instruments) 37
of which loss allowances established for trade accounts receivable (93)
of which loss allowances established for other receivables (4)
of which loss allowances established for cash and cash equivalents (1)
of which deferred taxes 18
Effects of IFRS 15 86
Retained earnings incl. net income as at January 1, 2018 26,894

B 8

Other Comprehensive Income Reconciliation (Fair-Value Measurement of Financial Instruments) € million

Fair-value measurement of financial instruments as at December 31, 2017
Reclassifications to retained earnings (37)
Remeasurement due to change in measurement category 11
Deferred taxes 9
Fair-value measurement of financial instruments as at January 1, 2018 81

IFRS 9 introduces new provisions for the classification and measurement of financial assets and replaces the current rules on the impairment of financial assets. The new standard requires a change in accounting methods for the effects resulting from a change in the company's own credit risk for financial liabilities classified at fair value and modifies the requirements for hedge accounting. The classification and measurement of financial liabilities is otherwise largely unchanged from the existing regulations.

Under IFRS 9, the classification and measurement of financial assets is determined by the company's business model and the characteristics of the cash flows of each financial asset. In the case of equity instruments held as of January 1, 2018, that are not held for trading, Bayer has uniformly opted to recognize future changes in their fair value through other comprehensive income in the statement of comprehensive income and to continue to classify these as equity upon the derecognition of the financial instrument. As for new instruments, Bayer can opt to make use of this option on an instrument-by-instrument basis upon recognition, but it must continue to do so thereafter.

As at the date of first-time application, reclassifications primarily resulted from the characteristics of the cash flows from fund shares, investments in limited partnerships, and the loan capital and jouissance right capital (Genussrechtkapital) provided to Bayer Pensionskasse VVaG. These financial instruments were previously reported in the category "available for sale," with changes in their fair value recognized in other comprehensive income in the statement of comprehensive income. They are now classified as debt instruments, and changes in their fair values are recognized through profit or loss.

Changes in the classification and measurement of financial assets led to the following effects as at the date of first-time application:

Financial Assets Reconciliation from IAS 39 to IFRS 9

€ million
Measurement category
in accordance with IAS 39
Carrying
amount
(IAS 39)
as of
Dec. 31, 2017
Reclassifi
cation
Remeasure
ment due to
change in
measurement
category
Remeasure
ment due to
implemen
tation of the
expected
loss model
Carrying
amount
(IFRS 9)
as of
Jan. 1, 2018
Measurement category
in accordance with IFRS 9
Trade accounts receivable Trade accounts receivable
Loans and receivables 8,582 (93) 8,489 Measured at amortized
cost
Other financial assets Other financial assets
Loans and receivables 1,731 1,731 Measured at
amortized cost
Available-for-sale financial
assets – debt instruments
34 34 Measured at
amortized cost
Held-to-maturity financial
assets
57 57 Measured at
amortized cost
Available-for-sale financial
assets – equity instruments
measured at amortized cost
35 11 46 Equity instruments
measured at fair value
through OCI (no recycling)
Available-for-sale financial
assets – equity instruments
measured at fair value
191 191 Equity instruments
measured at fair value
through OCI (no recycling)
Available-for-sale financial
assets – equity instruments
measured at fair value
39 39 Debt instruments
measured at fair value
through profit or loss
Available-for-sale financial
assets – debt instruments
2,429 145 2,574 Debt instruments
measured at fair value
through profit or loss
Derivatives that qualify
for hedge accounting
296 296 Derivatives that qualify
for hedge accounting
Derivatives that do not
qualify for hedge
accounting
351 351 Derivatives that do not
qualify for hedge
accounting
Other receivables Other receivables
Loans and receivables 380 (4) 376 Measured at
amortized cost
Available-for-sale financial
assets – debt instruments
46 46 Debt instruments
measured at fair value
through profit or loss
Cash and cash equivalents Cash and cash equivalents
Loans and receivables 7,581 (145) (1) 7,435 Measured at
amortized cost
Total financial assets 21,752 0 11 (98) 21,665

B 9

There were no effects on financial liabilities.

The following table shows the effects of the first-time application of IFRS 9 on retained earnings and other comprehensive income in the statement of other comprehensive income, broken down by measurement category:

B 10

Effects of First-Time Application of IFRS 9 on Retained Earnings and Other Comprehensive Income

Measurement category
in accordance with IFRS 9
Retained earnings
effect as of
Jan. 1, 2018
OCI effect as of
Jan. 1, 2018
Trade accounts receivable
Measured at amortized cost (93)
Other financial assets
Equity instruments measured at fair
value through OCI (no recycling)
11
Debt instruments measured at fair
value through profit or loss
10 (10)
Debt instruments measured at fair
value through profit or loss
36 (36)
Other receivables
Measured at amortized cost (4)
Debt instruments measured at fair
value through profit or loss
(9) 9
Cash and cash equivalents
Measured at amortized cost (1)
(61) (26)

The following table shows the effects of the first-time application of IFRS 9 on financial assets and liabilities that are based on unobservable inputs and are measured at fair value (Level 3). The development of these assets and liabilities in the first quarter of 2018 is presented in Table B 22.

B 11

Reconciliation of Financial Assets and Liabilities Measured at Fair Value (Level 3) from IAS 39 to IFRS 9

€ million
Measurement category
in accordance with IAS 39
Carrying
amount
(IAS 39)
as of
Dec. 31,
2017
Reclassi
fications
due to
change in
fair value
hierarchy
Remeasure
ments due
to change
in measure
ment
category
Carrying
amount
(IFRS 9)
as of
Jan. 1, 2018
Measurement category in
accordance with IFRS 9
Other financial assets Other financial assets
Available-for-sale financial
assets – equity instruments
measured at amortized cost
35 11 46 Equity instruments measured
at fair value through OCI
(no recycling)
Available-for-sale financial
assets – equity instruments
measured at fair value
18 4 22 Equity instruments measured
at fair value through OCI
(no recycling)
Available-for-sale financial
assets – equity instruments
measured at fair value
18 18 Debt instruments measured
at fair value through profit or
loss
Available-for-sale financial
assets – debt instruments
757 757 Debt instruments measured at
fair value through profit or loss
Derivatives 10 10 Derivatives
Other receivables Other receivables
Available-for-sale financial
assets – debt instruments
46 46 Debt instruments measured at
fair value through profit or loss
Total financial assets
(Level 3)
849 39 11 899 Total financial assets
(Level 3)
Other liabilities Other liabilities
Measured at fair value through
profit or loss (nonderivative)
(7) (7) Measured at fair value through
profit or loss (nonderivative)
Total financial liabilities
(Level 3)
(7) (7) Total financial liabilities
(Level 3)

Loss allowances for expected credit losses are recognized for financial assets measured at amortized cost. Expected lifetime credit losses for trade accounts receivable are recognized using the simplified approach. This is based on loss rates calculated from historical and forward-looking data, taking into account the business model, the respective customer and the economic environment of the geographical region. Receivables that are overdue by a significant amount of time – in some cases exceeding 90 days due to the customer structure – and receivables from debtors against which insolvency or similar proceedings have been initiated are tested individually for impairment. Expected credit losses for other financial assets are determined upon their first-time recognition primarily on the basis of credit default swaps, with losses for defaults within the next 12 months calculated using the Monte Carlo simulation method. In the event of a significant increase in default risk, expected lifetime credit losses are taken into account.

The effects from the increase in loss allowances from the first-time application of the new impairment model are presented in the following table:

B 12

Reconciliation of Loss Allowances

€ million
Measurement category in
accordance with IAS 39
Closing loss
allowances
under IAS 39
as at
Dec. 31, 2017
Remeasurement
due to
implementation
of the expected
loss model
under IFRS 9
Opening loss
allowances
under IFRS 9
as at Jan. 1, 2018
Measurement category in
accordance with IFRS 9
Trade accounts receivable Trade accounts receivable
Loans and receivables (425) (93) (518) Measured at amortized cost
Other receivables Other receivables
Loans and receivables (3) (4) (7) Measured at amortized cost
Cash and cash equivalents Cash and cash equivalents
Loans and receivables (1) (1) Measured at amortized cost
Total (428) (98) (526)

Changes in the fair values of financial liabilities measured at fair value through profit or loss resulting from Bayer's own credit risk are now recognized through other comprehensive income in the statement of comprehensive income rather than in the income statement. At Bayer, this change principally affects the debt instruments (exchangeable bond) issued in June 2017 which also can be exchanged into Covestro shares. As at the transition date, this accounting change did not have any material effects.

For hedge accounting, Bayer has opted to prospectively apply IFRS 9 from January 1, 2018. If only the intrinsic value of an option is designated as a hedging instrument in a hedging relationship, IFRS 9 requires that changes in the fair value of the time value of the options during the hedging period initially be recognized as other comprehensive income in the statement of comprehensive income. The release of the accumulated amounts, either in the form of a basis adjustment or directly through profit or loss, depends on the type of hedged transaction. In contrast to the other rules on hedge accounting, the revised accounting method is to be applied retrospectively. As at the transition date, these changes did not have any material impact on the presentation of the Group's financial position and results of operations.

The IASB issued IFRS 15 (Revenues from Contracts with Customers) in May 2014 and provided clarifications to the standard in April 2016. Both the standard and the clarifications have been endorsed by the European Union. IFRS 15 replaces the current IAS 18 (Revenue) and IAS 11 (Construction Contracts) revenue recognition standards and the related interpretations, and is applicable for annual reporting periods beginning on or after January 1, 2018. The new standard establishes a five-step model for revenue recognition from contracts with customers. Under IFRS 15, revenue is recognized at amounts that reflect the consideration that an entity expects to be entitled to in exchange for transferring goods or services to a customer. Revenue is recognized when (or as) the entity transfers control of goods or services to a customer either over time or at a point in time. In addition, IFRS 15 clarifies the allocation of individual topics to (new) line items in the statement of financial position and to functional cost items in the income statement, and whether gross or net amounts are to be presented.

As of January 1, 2018, Bayer transitioned to IFRS 15 on the basis of the modified retrospective method, accounting for the aggregate amount of the transition effects by way of an adjustment to retained earnings as of January 1, 2018, and presenting the comparative period in line with previous rules. Bayer has elected to retrospectively apply the standard only to contracts that are not completed contracts at the date of firsttime application, and has opted to reflect the aggregate effect of all contract modifications that occurred prior to the date of first-time application in accordance with IFRS 15.C7A(b).

The adoption of IFRS 15 has led to the following effects:

Changes in the timing of recognition

  • // IFRS 15 requires catch-up adjustments to revenue when milestone payments for right-to-access licenses become unconstrained leading to earlier revenue recognition. This change resulted in an increase in retained earnings by €64 million after deferred taxes and a decrease in contract liabilities (under IAS 18, amounts were presented as deferred income in other liabilities) by €86 million. For the Pharmaceuticals segment, the introduction of IFRS 15 translates into a €2 million decrease in quarterly net sales and a €1 million decrease in quarterly deferred tax expense as compared to IAS 18. Comparable quarterly effects will persist through 2027.
  • // IFRS 15 in conjunction with IAS 38 (Intangible Assets) generally requires the recognition of the purchase price related to a brand divestment net of associated carrying amounts in other operating income or expenses upon transfer of control. Some cases were identified where the purchase price was deferred under former policy in line with IAS 18, but would have been recognized in income earlier under IFRS 15, leading to a €21 million increase in retained earnings after deferred taxes and a €27 million decrease in contract liabilities (under IAS 18, amounts were presented as deferred income in other liabilities) on the date of transition. For the Animal Health segment, the introduction of IFRS 15 translates into a €7 million decrease in quarterly net sales and a €2 million decrease in quarterly deferred tax expense as compared to IAS 18. Quarterly effects will persist until early 2019, but at a lower level. For the Pharmaceuticals segment, this change effective January 1, 2018, led to a one-time decrease of €6 million in quarterly net sales in the first quarter of 2018 and a €1 million decrease in quarterly tax expense as compared to IAS 18. An additional divestment attributable to the Pharmaceuticals segment that was completed in the first quarter of 2018 gave rise to a €2 million decrease in net sales and a €14 million increase in other operating income as compared to IAS 18. Net sales will decrease by this difference – €12 million – over the remaining quarters of 2018 as compared to IAS 18.
  • // Including the effects described individually, the change in the timing of revenue recognition led to a €2 million decrease in quarterly earnings as compared to revenue recognition under IAS 18.

Presentational changes

Bayer also changed the presentation of certain items in the statement of financial position and income statements to reflect the methodology of IFRS 15.

  • // IFRS 15 changes the presentation of expected product returns within the statement of financial position from net to gross in cases where returns are expected to be resalable and Bayer will refund the purchase price. The right-of-return asset is reflected in inventories at the former carrying amount less expected costs to recover and potential impairment. The refund liabilities include amounts expected to be refunded upon product return. Prior to the adoption of IFRS 15, Bayer presented the margin of expected returns on a net basis in "other provisions." In the statement of cash flows, the increase in inventories to be recorded under IFRS 15 is set against a decline in "other working capital, other noncash items."
  • // Amounts already received (or receivable), but expected to be refunded to the customer are presented as "refund liabilities" under IFRS 15. These amounts typically relate to expected volume rebates and expected product returns and were previously presented as "other provisions."
  • // Advance payments received (or receivable) in connection with product deliveries were previously recognized in trade accounts payable. Advance payments received (or receivable) relating to right-toaccess licenses and service contracts recognized over time were previously presented under "deferred income" in "other liabilities." With the introduction of IFRS 15, both are presented as contract liabilities. Within the statement of cash flows, the decline in trade accounts payable resulting from the presentational change is set against a corresponding change in "other working capital, other noncash items."

The effects of applying the modified retrospective method on the opening statement of financial position as at January 1, 2018, are shown in table B13. In addition, table B 14 presents the impact on the Group statement of financial position as at March 31, 2018, that the continued application of IAS 18 would have had compared with IFRS 15.

B 13

IFRS 15 Accounting Changes: Consolidated Statements of Financial Position as of January 1, 2018
Dec. 31, 2017 Jan. 1, 2018
Before
accounting
changes
Presentational
changes
Changes in
timing of
recognition
After
accounting
changes
€ million
Noncurrent assets
Deferred taxes 4,915 (5) 4,910
Other noncurrent assets 40,099 40,099
45,014 (5) 45,009
Current assets
Inventories 6,550 76 6,626
Other current assets 23,523 23,523
30,073 76 30,149
Total assets 75,087 76 (5) 75,158
Equity
Other reserves 25,026 86 25,112
Other equity 11,835 11,835
36,861 86 36,947
Noncurrent liabilities
Other provisions 1,366 (152) 1,214
Refund liabilities 152 152
Contract liabilities 905 (78) 827
Other liabilities 1,116 (905) 211
Deferred taxes 1,153 24 1,177
Other noncurrent liabilities 20,998 20,998
24,633 0 (54) 24,579
Current liabilities
Other provisions 4,344 (2,197) 2,147
Refund liabilities 2,275 2,275
Contract liabilities 740 (37) 703
Trade accounts payable 5,129 (561) 4,568
Other liabilities 1,652 (181) 1,471
Other current liabilities 2,468 2,468
13,593 76 (37) 13,632
Total equity and liabilities 75,087 76 (5) 75,158
IFRS 15
March 31,
2018
Presentational
changes
Changes in
timing of
recognition
IAS 18
March 31,
2018
€ million
Noncurrent assets
Deferred taxes 4,384 2 4,386
Other noncurrent assets 37,841 37,841
42,225 2 42,227
Current assets
Inventories 6,402 (52) 6,350
Other current assets 26,767 26,767
33,169 (52) 33,117
Total assets 75,394 (52) 2 75,344
Equity
Other reserves 26,553 (84) 26,469
Other equity 11,831 11,831
38,384 (84) 38,300
Noncurrent liabilities
Other provisions 1,302 146 1,448
Refund liabilities 146 (146) -
Contract liabilities 799 (799) -
Other liabilities 228 799 73 1,100
Deferred taxes 586 (23) 563
Other noncurrent liabilities 21,796 20,851
23,912 0 50 23,962
Current liabilities
Other provisions 2,194 2,467 4,661
Refund liabilities 2,519 (2,519) -
Contract liabilities 197 (197) -
Trade accounts payable 3,943 71 4,014
Other liabilities 1,318 126 36 1,480
Other current liabilities 5,643 2,927
13,098 (52) 36 13,082
Total equity and liabilities 75,394 (52) 2 75,344

B 14

Change in accounting methods

In connection with the planned acquisition of Monsanto and in preparation for the future combined business, the structure of the Crop Science segment was adjusted as of January 1, 2018, in line with the internal financial reporting system (management approach). In the new structure, all the strategic business entities are organizationally located directly below the Crop Science segment. Global impairment testing will also be carried out at the Crop Science segment level each year in the future.

Changes in underlying parameters

Changes in the underlying parameters relate primarily to currency exchange rates and the interest rates used to calculate pension obligations.

The exchange rates for major currencies against the euro varied as follows:

B 15
Exchange Rates for Major Currencies
Closing rate Average rate
€1 Dec. 31, 2017 March 31, 2017 March 31, 2018 Q1 2017 Q1 2018
BRL Brazil 3.98 3.37 4.09 3.35 3.99
CAD Canada 1.51 1.43 1.59 1.41 1.55
CHF Switzerland 1.17 1.07 1.18 1.07 1.17
CNY China 7.81 7.35 7.73 7.31 7.81
GBP United Kingdom 0.89 0.86 0.88 0.86 0.88
JPY Japan 135.01 119.46 131.19 121.07 133.17
MXN Mexico 23.66 20.01 22.52 21.61 23.05
RUB Russia 69.41 60.28 70.85 62.59 69.90
USD United States 1.20 1.07 1.23 1.06 1.23

The most important interest rates used to calculate the present value of pension obligations are given below:

B 16
Dec. 31, 2017 March 31, 2018
1.90 1.90
2.50 2.60
3.40 3.80

Segment reporting

As of March 31, 2018, the Bayer Group comprises the four reportable segments Pharmaceuticals, Consumer Health, Crop Science and Animal Health.

The following table shows the reconciliation of EBITDA before special items of the above-mentioned segments and the reconciliation to income before income taxes of the Group from continuing operations:

B17
Reconciliation of Segments' EBITDA Before Special Items
to Group Income Before Income Taxes
€ million Q1 2017 Q1 2018
EBITDA before special items of segments 3,189 2,996
EBITDA before special items of Corporate Functions and Consolidation (135) (100)
EBITDA before special items1 3,054 2,896
Depreciation, amortization and impairment losses before special items of segments (522) (504)
Depreciation, amortization and impairment losses before special items
of Corporate Functions and Consolidation
(3) (4)
Depreciation, amortization and impairment losses before special items (525) (508)
EBIT before special items of segments 2,667 2,492
EBIT before special items of Corporate Functions and Consolidation (138) (104)
EBIT before special items
1
2,529 2,388
Special items of segments (100) (75)
Special items of Corporate Functions and Consolidation (2) (3)
Special items 1 (102) (78)
EBIT of segments 2,567 2,417
EBIT of Corporate Functions and Consolidation (140) (107)
EBIT1 2,427 2,310
Financial result (296) 130
Income before income taxes 2,131 2,440

2017 figures restated 1 For definition see Annual Report 2017, A 2.4 "Alternative Performance Measures Used by the Bayer Group."

Scope of consolidation

Changes in the scope of consolidation

The consolidated financial statements as of March 31, 2018, included 237 companies (December 31, 2017: 237 companies). Eight (December 31, 2017: eight) joint ventures and four (December 31, 2017: four) associates were accounted for in the consolidated financial statements using the equity method according to IAS 28 (Investments in Associates and Joint Ventures). The Covestro Group was deconsolidated as of September 30, 2017. As the parent company of the Covestro Group, Covestro AG is accounted for in the consolidated financial statements using the equity method.

Acquisitions, divestments and discontinued operations

Planned acquisitions

With regard to the planned acquisition of Monsanto, we refer to the Annual Report 2017. Following the approval by the authorities in Brazil, China and the European Union of the planned acquisition of Monsanto by Bayer, nearly two-thirds of the approvals have been granted. Closing of the transaction is currently expected in the second quarter of 2018.

Divestments and discontinued operations

Bayer ceded de facto control of Covestro and deconsolidated the company at the end of September 2017. As of the loss of control, Covestro fulfills the conditions for presentation as a discontinued operation. In connection with the sale of Covestro AG shares in 2017, Bayer AG entered into derivative contracts. These resulted in Bayer AG retaining economic exposure to the price of Covestro AG shares. In the first quarter of 2018, Bayer generated income after income taxes of €8 million from these contracts.

B 18

Income Statements for Discontinued Operations
-- -- -- ----------------------------------------------- --
Covestro Diabetes Care Total
€ million Q1 2017 Q1 2018 Q1 2017 Q1 2018 Q1 2017 Q1 2018
Net sales 3,564 128 3,692
Cost of goods sold (2,358) (7) (2,365)
Gross profit 1,206 121 1,327
Selling expenses (346) (1) (347)
Research and development expenses (64) (64)
General administration expenses (112) (2) (114)
Other operating income / expenses 5 10 5 10 10
EBIT1 689 10 123 812 10
Financial result (53) (53)
Income before income taxes 636 10 123 759 10
Income taxes (171) (2) (24) (195) (2)
Income after income taxes 465 8 99 564 8
of which attributable
to noncontrolling interest
190 190
of which attributable to Bayer AG
stockholders (net income)
275 8 99 374 8

1 For definition see Bayer Annual Report 2017, A 2.4 "Alternative Performance Measures Used by the Bayer Group."

In the first quarter of 2018, the discontinued operations affected the Bayer Group statement of cash flows as follows:

B 19
Cash Flows from Discontinued Operations
Covestro Diabetes Care Total
€ million Q1 2017 Q1 2018 Q1 2017 Q1 2018 Q1 2017 Q1 2018
Net cash provided
by (used in) operating activities
275 15 290
Net cash provided
by (used in) investing activities
(112) (112)
Net cash provided
by (used in) financing activities
(1) (15) (16)
Change in cash and cash equivalents 162 162

As no cash was assigned to the discontinued operation Diabetes Care, the balance of the cash provided is deducted again in financing activities.

Assets held for sale

In connection with the planned acquisition of Monsanto, Bayer signed an agreement with BASF on October 13, 2017, concerning the sale of selected Crop Science businesses. The businesses to be sold comprise Bayer's global glufosinate ammonium business and the related LibertyLink™ technology for herbicide tolerance and a substantial part of the field crop seed business, including the related research and development capabilities. The seeds business being divested includes the global cotton seed business (excluding India and South Africa), the North American and European canola seed business, and the soybean seed business. The agreed base purchase price of €5.9 billion excludes the value of any net working capital and is subject to the customary adjustment mechanisms.

In connection with the planned acquisition of Monsanto and the associated merger control proceedings, Bayer has undertaken to divest, in addition to the divestments detailed above, its entire vegetable seeds business, its R&D platform for hybrid wheat, its remaining canola seed business, three research projects in the area of nonselective herbicides, its global digital farming business and business activities in the field of seed treatments. BASF is the intended purchaser of these assets.

The transactions are subject to regulatory approval as well as the successful closing of Bayer's acquisition of Monsanto. Bayer will continue to own, operate and maintain these businesses until the closing of these divestments.

On January 30, 2018, the Pharmaceuticals Division signed agreements to sell its MK Generics business in Central America and the Caribbean to Tecnoquímicas S.A. The business to be sold includes the Bonima production plant in El Salvador. The base purchase price is €44 million.

The assets and liabilities held for sale are presented below:

B 20
€ million March 31, 2018
Goodwill 587
Other intangible assets 380
Property, plant and equipment 1,277
Other assets 334
Deferred taxes 135
Inventories 413
Cash and cash equivalents 6
Assets held for sale 3,132
Provisions for pensions and other post-employment benefits 37
Other provisions 44
Financial liabilities 15
Other liabilities 376
Deferred taxes 48
Liabilities directly related to assets held for sale 520

Financial instruments

The following table shows the carrying amounts and fair values of financial assets and liabilities by category of financial instrument under IFRS 9 and a reconciliation to the corresponding line items in the statements of financial position. Since the line items "Trade accounts receivable," "Other receivables" and "Other liabilities" contain both financial instruments and nonfinancial assets or liabilities (such as other tax receivables or advance payments for services to be received in the future), the reconciliation is shown in the column headed "Nonfinancial assets /liabilities."

The transition effects from the reclassification and remeasurement of financial assets upon the first-time application of IFRS 9 are detailed in the section "Financial reporting standards applied for the first time in 2018."

Carrying Amounts and Fair Values of Financial Instruments

March 31, 2018
Measured at
amortized
cost
Measured at fair value
[fair value for information 1]
Nonfinancial
assets /
liabilities
Based on
quoted prices
in active
markets
(Level 1)
Based on
observable
market data
(Level 2)
Based on
unobservable
inputs
(Level 3)
€ million Carrying
amount
Carrying
amount
Carrying
amount
Carrying
amount
Carrying
amount
Carrying
amount
in the
statement
of financial
position
Trade accounts receivable 9,343 155 9,498
Measured at amortized cost 9,343 9,343
Nonfinancial assets 155 155
Other financial assets 322 2,930 4,958 842 9,052
Measured at amortized cost 322 [322] 322
Measured at fair value through profit or loss 2,655 4,371 775 7,801
Measured at fair value through OCI (no
recycling)
275 53 328
Derivatives 587 14 601
Other receivables 313 50 1,201 1,564
Measured at amortized cost 313 [313] 313
Measured at fair value through profit or loss 50 50
Nonfinancial assets 1,201 1,201
Cash and cash equivalents 5,332 5,332
Measured at amortized cost 5,332 [5,332] 5,332
Total financial assets 15,310 2,930 4,958 892 24,090
of which measured at amortized cost 15,310 15,310
of which measured at fair value through
profit or loss
2,655 4,371 825 7,851
Financial liabilities 12,656 1,179 199 14,034
Measured at amortized cost 12,656 [11,030] [1,991] 12,656
Measured at fair value through profit or loss
(nonderivative)
1,179 1,179
Derivatives 199 199
Trade accounts payable 3,943 3,943
Measured at amortized cost 3,943 3,943
Other liabilities 647 194 5 700 1,546
Measured at amortized cost 647 [647] 647
Measured at fair value through profit or loss
(nonderivative)
5 5
Derivatives 194 194
Nonfinancial liabilities 700 700
Total financial liabilities 17,246 1,179 393 5 18,823
of which measured at amortized cost 17,246 17,246
of which measured at fair value through
profit or loss (nonderivative)
1,179 5 1,184
of which derivatives 393 393

Fair value of the financial instruments measured at amortized cost; the exemption provisions under IFRS 7.29(a) were applied for information on specific fair values.

B 21

The category "measured at amortized cost" within other financial assets and in financial liabilities also includes receivables and liabilities under finance leases in which Bayer is the lessor or lessee and which are therefore measured in accordance with IAS 17.

Due to the short maturities of most trade accounts receivable and payable, other receivables and liabilities, and cash and cash equivalents, their carrying amounts at the closing date do not significantly differ from the fair values.

The fair values of financial assets and liabilities measured at amortized cost that are given for information are the present values of the respective future cash flows. The present values are determined by discounting the cash flows at a closing-date interest rate, taking into account the term of the assets or liabilities and the creditworthiness of the counterparty. Where a market price is available, however, this is deemed to be the fair value.

The fair values of financial assets measured at fair value correspond to quoted prices in active markets (Level 1), or are determined using valuation techniques based on observable market data as of the end of the reporting period (Level 2) or are the present values of the respective future cash flows, determined on the basis of unobservable inputs (Level 3).

The fair values of derivatives for which no publicly quoted prices exist in active markets (Level 1) are determined using valuation techniques based on observable market data as of the end of the reporting period (Level 2). In applying valuation techniques, credit value adjustments are determined to allow for the contracting party's credit risk.

Currency and commodity forward contracts are measured individually at their forward rates or forward prices on the closing date. These depend on spot rates or prices, including time spreads. The fair values of interest-rate hedging instruments and cross-currency interest-rate swaps were determined by discounting future cash flows over the remaining terms of the instruments at market rates of interest, taking into account any foreign currency translation as of the closing date.

Fair values measured using unobservable inputs are categorized within Level 3 of the fair value hierarchy. This applies to certain debt or equity instruments, in some cases to the fair values of embedded derivatives, and to obligations for contingent consideration in business combinations. Credit risk is frequently the principal unobservable input used to determine the fair values of debt instruments classified as measured at fair value by the discounted cash flow method. Here the credit spreads of comparable issuers are applied. A significant increase in credit risk could result in a lower fair value, whereas a significant decrease could result in a higher fair value. However, a relative change of 10% in the credit spread does not materially affect the fair value.

Embedded derivatives are separated from their respective host contracts, provided they are not financial instruments. Such host contracts are generally sale or purchase agreements relating to the operational business. The embedded derivatives cause the cash flows from the contracts to vary with exchange-rate or price fluctuations. The internal measurement of embedded derivatives is mainly performed using the discounted cash flow method, which is based on unobservable inputs. These include planned sales and purchase volumes, and prices derived from market data. Regular monitoring is carried out based on these fair values as part of quarterly reporting.

The financial liabilities arising from the debt instruments (exchangeable bond) issued in June 2017 that can be converted into Covestro shares are measured at fair value through profit or loss. This exchangeable bond is a hybrid financial instrument containing a debt instrument as a nonderivative host contract and multiple embedded derivatives.

The changes in the amount of financial assets and liabilities recognized at fair value based on unobservable inputs (Level 3) for each financial instrument category were as follows:

B 22

Development of Financial Assets and Liabilities (Level 3)
2018
€ million Financial
assets
at fair value
through
profit or loss
Financial
assets
at fair value
through OCI
(no
recycling)
Derivatives
(net)
Liabilities
measured at
fair value
(non
derivative)
Total
Carrying amounts of net assets
(net liabilities), January 1
821 68 10 (7) 892
Gains (losses) recognized in profit or loss 3 4 7
of which related to assets /liabilities
recognized in the statements of financial
position
3 4 7
Gains (losses) recognized outside profit or loss (4) (4)
Additions of assets (liabilities) 1 1
Settlements of (assets) liabilities (1) 1
Transfers (IFRS 5) (6) 1 (5)
Disposals from divestments / changes in scope
of consolidation
(4) (4)
Carrying amounts of net assets
(net liabilities), March 31
825 53 14 (5) 887

The changes recognized in profit or loss were included in other operating income / expenses, as well as in the financial result in interest income and in other financial income and expenses.

The following table shows the carrying amounts and fair values of financial assets and liabilities by category of financial instrument as of December 31, 2017, under IAS 39.

B 23

Carrying Amounts and Fair Values of Financial Instruments

Dec. 31, 2017
Measured at
amortized
Nonfinancial
Measured at fair value
assets /
cost [fair value for information 1] liabilities
Based on
quoted prices
in active
markets
(Level 1)
Based on
observable
market data
(Level 2)
Based on
unobservable
inputs
(Level 3)
€ million Carrying
amount
Carrying
amount
Carrying
amount
Carrying
amount
Carrying
amount
Carrying
amount
in the
statement
of financial
position
Trade accounts receivable 8,582 8,582
Loans and receivables 8,582 8,582
Other financial assets 1,823 452 2,085 803 5,163
Loans and receivables 1,731 [1,731] 1,731
Available-for-sale financial assets 35 448 1,452 793 2,728
Held-to-maturity financial assets 57 [58] 57
Derivatives 4 633 10 647
Other receivables 380 46 1,250 1,676
Loans and receivables 380 [380] 380
Available-for-sale financial assets 46 46
Nonfinancial assets 1,250 1,250
Cash and cash equivalents 7,581 7,581
Loans and receivables 7,581 [7,581] 7,581
Total financial assets 18,366 452 2,085 849 21,752
of which loans and receivables 18,274 18,274
of which available-for-sale financial assets 35 448 1,452 839 2,774
Financial liabilities 12,958 1,220 240 14,418
Measured at amortized cost 12,958 [11,327] [2,183] 12,958
Measured at fair value (nonderivative) 1,220 1,220
Derivatives 240 240
Trade accounts payable 4,568 561 5,129
Measured at amortized cost 4,568 4,568
Nonfinancial liabilities 561 561
Other liabilities 681 2 319 7 1,759 2,768
Measured at amortized cost 681 [681] 681
Measured at fair value (nonderivative) 7 7
Derivatives 2 319 321
Nonfinancial liabilities 1,759 1,759
Total financial liabilities 18,207 1,222 559 7 19,995
of which measured at amortized cost 18,207 18,207
of which derivatives 2 559 561

1 Fair value of the financial instruments measured at amortized cost; the exemption provisions under IFRS 7.29(a) were applied for information on specific fair values. The following table shows the changes in the amounts of financial assets and liabilities recognized at fair value based on unobservable inputs (Level 3) for each financial instrument category for the comparative period under IAS 39:

B 24

Development of Financial Assets and Liabilities (Level 3)

2017
€ million Available
for-sale
financial
assets
Derivatives
(net)
Liabilities
measured at
fair value
(non
derivative)
Total
Carrying amounts of net assets (net liabilities), January 1 851 (8) (8) 835
Gains (losses) recognized in profit or loss 4 3 7
of which related to assets /liabilities recognized
in the statements of financial position
4 3 7
Gains (losses) recognized outside profit or loss (18) (18)
Additions of assets (liabilities) 3 3
Settlements of (assets) liabilities
Carrying amounts of net assets (net liabilities), March 31 840 (5) (8) 827

Contingent liabilities and other financial commitments

The Group's contingent liabilities amounted to €844 million as of March 31, 2018, and mainly comprised pending legal cases in several countries. Other financial liabilities totaling €52,260 million mainly resulted from the definitive merger agreement with Monsanto Company of September 14, 2016, that concerns a sum of €45,673 million and provides for Bayer's acquisition of all outstanding shares in Monsanto Company against a cash payment of US\$128 per share.

Legal Risks

To find out more about the Bayer Group's legal risks, please see Note 32 to the consolidated financial statements in the Bayer Annual Report 2017, which can be downloaded free of charge at www.bayer.com. Since the Bayer Annual Report 2017, the following significant changes have occurred in respect of the legal risks:

Mirena™: As of April 13, 2018, lawsuits from approximately 3,100 users of Mirena™, an intrauterine system providing long-term contraception, had been served upon Bayer in the United States. Plaintiffs allege personal injuries resulting from the use of Mirena™, including perforation of the uterus, ectopic pregnancy or idiopathic intracranial hypertension, and seek compensatory and punitive damages. Additional lawsuits are anticipated. As of April 13, 2018, lawsuits from approximately 480 users of Mirena™ alleging idiopathic intracranial hypertension had been served upon Bayer in the United States.

In April 2018, the Master Settlement Agreement regarding the global settlement of the perforation cases for a total amount of US\$12.2 million was executed. Bayer may withdraw from the agreement if fewer than 98% of those who are eligible choose to participate. As of April 13, 2018, a total of approximately 4,100 cases would be included in the settlement.

Xarelto™: As of April 13, 2018, U.S. lawsuits from approximately 23,200 recipients of Xarelto™, an oral anticoagulant for the treatment and prevention of blood clots, had been served upon Bayer. Plaintiffs allege that users have suffered personal injuries from the use of Xarelto™, including cerebral, gastrointestinal or other bleeding and death, and seek compensatory and punitive damages. Additional lawsuits are anticipated. As of April 13, 2018, ten Canadian lawsuits relating to Xarelto™ seeking class action certification had been served upon Bayer.

Essure™: As of April 13, 2018, U.S. lawsuits from approximately 16,800 users of Essure™, a medical device offering permanent birth control with a nonsurgical procedure, had been served upon Bayer. Plaintiffs allege personal injuries from the use of Essure™, including hysterectomy, perforation, pain, bleeding, weight gain, nickel sensitivity, depression and unwanted pregnancy, and seek compensatory and punitive damages. Additional lawsuits are anticipated. As of April 13, 2018, two Canadian lawsuits relating to Essure™ seeking class action certification had been served upon Bayer.

Class actions over neonicotinoids in Canada: In February 2018, a court in Quebec certified a class proposed by plaintiffs. Plaintiffs are honey producers in Quebec claiming damages and punitive damages and alleging Bayer and another crop protection company were negligent in the design, development, marketing and sale of neonicotinoid pesticides.

Betaferon™/Betaseron™: Since 2010, Bayer and Biogen Idec MA Inc. have been engaged in a dispute in the United States about the validity of a patent issued to Biogen and whether Bayer's production and distribution of Betaseron™ would infringe such patent. Betaseron™ is Bayer's drug product for the treatment of multiple sclerosis. In February 2018, a jury decided that Biogen's patent is invalid at the end of a trial regarding Biogen's claims against EMD Serono, Inc. and Pfizer Inc. for infringement of the same patent. Biogen has challenged the jury's verdict. Unless the jury's verdict is overturned, Biogen cannot assert its claims against Bayer.

Related parties

Related parties as defined in IAS 24 (Related Party Disclosures) are those legal entities and natural persons that are able to exert influence on Bayer AG and its subsidiaries or over which Bayer AG or its subsidiaries exercise control or joint control or have a significant influence. They include, in particular, nonconsolidated subsidiaries, joint ventures and associates included in the consolidated financial statements at cost of acquisition or using the equity method, post-employment benefit plans and the corporate officers of Bayer AG.

Sales to related parties were not material from the viewpoint of the Bayer Group. Liabilities to joint ventures declined by €0.1 billion to €0.1 billion compared with December 31, 2017, and primarily pertained to the joint venture Casebia Therapeutics Limited Liability Partnership, Ascot, United Kingdom, which was established together with CRISPR Therapeutics AG, Basel, Switzerland.

Events After the End of the Reporting Period

Temasek subscribes to capital increase and acquires approximately 3.6% of Bayer

In April 2018, the investment company Temasek, Singapore, subscribed to 31 million new shares of Bayer, corresponding to around 3.6% of the increased capital stock, for total gross proceeds of €3 billion. The proceeds from this capital increase were used to reduce the syndicated credit facility arranged for financing the planned acquisition of Monsanto by US\$ 3.7 billion to US\$46 billion.

In light of the planned acquisition of Monsanto, Bayer signed an agreement to sell further Crop Science businesses to BASF on April 24, 2018. The businesses being divested include in particular the global vegetable seeds business, certain seed treatments, the research platform for wheat hybrids and certain glyphosate-based herbicides in Europe. In addition, three research projects in the field of total herbicides and Bayer's digital farming business will also be transferred. In return, Bayer will receive a back license for certain digital farming applications.

Leverkusen, April 26, 2018 Bayer Aktiengesellschaft

The Board of Management

Werner Baumann

Liam Condon Johannes Dietsch Dr. Hartmut Klusik

Kemal Malik Wolfgang Nickl Heiko Schipper

Dieter Weinand

Review Report

To Bayer Aktiengesellschaft, Leverkusen /Germany

We have reviewed the condensed interim consolidated financial statements – comprising the income statement and the statement of comprehensive income, the statement of financial position, the statement of cash flows, the condensed statement of changes in equity as well as selected explanatory notes to the financial statements – and the interim group management report for the period from 1 January until 31 March 2018 of Bayer Aktiengesellschaft, Leverkusen, that are part of the quarterly financial report under § 115 WpHG (Wertpapierhandelsgesetz: German Securities Trading Act). The preparation of the condensed interim consolidated financial statements in accordance with the International Financial Reporting Standards (IFRS) applicable to interim financial reporting as adopted by the EU and of the interim group management report in accordance with the requirements of the WpHG applicable to interim group management reports is the responsibility of the entity's Management Board. Our responsibility is to issue a report on the condensed interim consolidated financial statements and on the interim group management report based on our review.

We conducted our review of the interim consolidated financial statements and of the interim group management report in accordance with the German generally accepted standards for the review of financial statements promulgated by the Institut der Wirtschaftsprüfer (Institute of Public Auditors in Germany) as well as in supplementary compliance with the International Standard on Review Engagements "Review of Interim Financial Information performed by the Independent Auditor of the Entity" (ISRE 2410). Those standards require that we plan and perform the review such that we can preclude through critical evaluation, with a limited level of assurance, that the condensed interim consolidated financial statements have not been prepared, in all material respects, in accordance with the IFRS applicable to interim financial reporting as adopted by the EU, or that the interim group management report has not been prepared, in material respects, in accordance with the requirements of the WpHG applicable to interim group management reports. A review is limited primarily to inquiries of personnel of the entity and analytical assessments and therefore does not provide the assurance attainable in a financial statement audit. Since, in accordance with our engagement, we have not performed a financial statement audit, we cannot issue an auditor's report.

Based on our review, no matters have come to our attention that cause us to presume that the condensed interim consolidated financial statements of Bayer Aktiengesellschaft, Leverkusen, have not been prepared, in all material respects, in accordance with the IFRS applicable to interim financial reporting as adopted by the EU, or that the group management report has not been prepared, in material respects, in accordance with the requirements of the WpHG applicable to interim group management reports.

Munich, Germany, 27 April 2018

Deloitte GmbH Wirtschaftsprüfungsgesellschaft

Heiner Kompenhans Prof. Dr. Frank Beine Wirtschaftsprüfer Wirtschaftsprüfer (German Public Auditor) (German Public Auditor)

Financial Calendar

Annual Stockholders' Meeting 2018 May 25, 2018
Planned dividend payment day May 30, 2018
Q2 2018 Interim Report September 5, 2018
Q3 2018 Interim Report November 13, 2018
Annual Report 2018 February 27, 2019
Q1 2019 Interim Report April 25, 2019
Annual Stockholders' Meeting 2019 April 26, 2019

Masthead

Published by Bayer AG, 51368 Leverkusen, Germany

Editor Meike Kneip, phone +49 214 30 20015 Email: [email protected]

Investor Relations Peter Dahlhoff, phone +49 214 30 33022 Email: [email protected]

English edition Bayer Business Services GmbH Translation Services

Date of publication Thursday, May 3, 2018

Bayer on the internet www.bayer.com

ISSN 0343 / 1975

Interim Group Management Report and Condensed Consolidated Interim Financial Statements produced in-house with FIRE.sys.

Cautionary Statements Regarding Forward-Looking Information

Certain statements contained in this communication may constitute "forward-looking statements." Actual results could differ materially from those projected or forecast in the forward-looking statements. The factors that could cause actual results to differ materially include the following: uncertainties as to the timing of the transaction; the possibility that the parties may be unable to achieve expected synergies and operating efficiencies in the merger within the expected time frames or at all and to successfully integrate Monsanto's operations into those of Bayer; such integration may be more difficult, time-consuming or costly than expected; revenues following the transaction may be lower than expected; operating costs, customer loss and business disruption (including, without limitation, difficulties in maintaining relationships with employees, customers, clients or suppliers) may be greater than expected following the announcement of the transaction; the retention of certain key employees at Monsanto; risks associated with the disruption of management's attention from ongoing business operations due to the transaction; the conditions to the completion of the transaction may not be satisfied, or the regulatory approvals required for the transaction may not be obtained on the terms expected or on the anticipated schedule; the parties' ability to meet expectations regarding the timing, completion and accounting and tax treatments of the merger; the impact of the refinancing of the loans taken out for the transaction, the impact of indebtedness incurred by Bayer in connection with the transaction and the potential impact on the rating of indebtedness of Bayer; the effects of the business combination of Bayer and Monsanto, including the combined company's future financial condition, operating results, strategy and plans; other factors detailed in Monsanto's Annual Report on Form 10-K filed with the SEC for the fiscal year ended August 31, 2017 and Monsanto's other filings with the SEC, which are available at http://www.sec.gov and on Monsanto's website at www.monsanto.com; and other factors discussed in Bayer's public reports which are available on the Bayer website at www.bayer.com. Bayer and Monsanto assume no obligation to update the information in this communication, except as otherwise required by law. Readers are cautioned not to place undue reliance on these forward-looking statements that speak only as of the date.

Legal Notice

The product names designated with ™ are brands of the Bayer Group or our distribution partners and are registered trademarks in many countries.

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